Cargando…

Mitochondrial DNA haplogroup distribution in Chaoshanese with and without myopia

PURPOSE: Mitochondrial DNA (mtDNA) haplogroups affect the clinical expression of Leber hereditary optic neuropathy, age-related macular degeneration, and other diseases. The objective of this study is to investigate whether an mtDNA background is associated with myopia. METHODS: Blood DNA was obtain...

Descripción completa

Detalles Bibliográficos
Autores principales:	Wang, Qin, Wang, Panfeng, Li, Shiqiang, Xiao, Xueshan, Jia, Xiaoyun, Guo, Xiangming, Kong, Qing-Peng, Yao, Yong-Gang, Zhang, Qingjiong
Formato:	Texto
Lenguaje:	English
Publicado:	Molecular Vision 2010
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2830021/ https://www.ncbi.nlm.nih.gov/pubmed/20208987

Ejemplares similares

Mitochondrial DNA Haplogroup Background Affects LHON, but Not Suspected LHON, in Chinese Patients
por: Zhang, A-Mei, et al.
Publicado: (2011)

Mitochondrial DNA Haplogroup Confers Genetic Susceptibility to Nasopharyngeal Carcinoma in Chaoshanese from Guangdong, China
por: Hu, Sheng-Ping, et al.
Publicado: (2014)

An evaluation of OPTC and EPYC as candidate genes for high myopia
por: Wang, Panfeng, et al.
Publicado: (2009)

Sequence variations of GRM6 in patients with high myopia
por: Xu, Xiaoyu, et al.
Publicado: (2009)

Replication study of significant single nucleotide polymorphisms associated with myopia from two genome-wide association studies
por: Wang, Qin, et al.
Publicado: (2011)

Mitochondrial DNA Sequence Variation and Haplogroup Distribution in Chinese Patients with LHON and m.14484T>C
por: Yu, Dandan, et al.
Publicado: (2010)

X-linked heterozygous mutations in ARR3 cause female-limited early onset high myopia
por: Xiao, Xueshan, et al.
Publicado: (2016)

A recurrent mutation in GUCY2D associated with autosomal dominant cone dystrophy in a Chinese family
por: Xiao, Xueshan, et al.
Publicado: (2011)

Mutations in NYX of individuals with high myopia, but without night blindness
por: Zhang, Qingjiong, et al.
Publicado: (2007)

CPSF1 mutations are associated with early-onset high myopia and involved in retinal ganglion cell axon projection
por: Ouyang, Jiamin, et al.
Publicado: (2019)

Evaluation of EGR1 as a candidate gene for high myopia
por: Li, Tuo, et al.
Publicado: (2008)

Novel RS1 mutations associated with X-linked juvenile retinoschisis
por: YI, JUNHUI, et al.
Publicado: (2012)

Mutation survey of the optic atrophy 1 gene in 193 Chinese families with suspected hereditary optic neuropathy
por: Chen, Yabin, et al.
Publicado: (2013)

Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism
por: Wang, Yingwei, et al.
Publicado: (2023)

Exome sequencing identified null mutations in LOXL3 associated with early-onset high myopia
por: Li, Jiali, et al.
Publicado: (2016)

Association of markers at chromosome 15q14 in Chinese patients with moderate to high myopia
por: Jiao, Xiaodong, et al.
Publicado: (2012)

Novel BMP4 Truncations Resulted in Opposite Ocular Anomalies: Pathologic Myopia Rather Than Microphthalmia
por: Jiang, Yi, et al.
Publicado: (2021)

An Early Diagnostic Clue for COL18A1- and LAMA1-Associated Diseases: High Myopia With Alopecia Areata in the Cranial Midline
por: Wang, Panfeng, et al.
Publicado: (2021)

PAX3 mutations and clinical characteristics in Chinese patients with Waardenburg syndrome type 1
por: Wang, Juan, et al.
Publicado: (2010)

Mutational screening of 10 genes in Chinese patients with microphthalmia and/or coloboma
por: Zhang, Xiaohui, et al.
Publicado: (2009)

Mutation spectrum of PAX6 in Chinese patients with aniridia
por: Zhang, Xiaohui, et al.
Publicado: (2011)

Evaluation of MFRP as a candidate gene for high hyperopia
por: Wang, Panfeng, et al.
Publicado: (2009)

Identification of FZD4 and LRP5 mutations in 11 of 49 families with familial exudative vitreoretinopathy
por: Yang, Huiqin, et al.
Publicado: (2012)

Phenotypic characterization of patients with early-onset high myopia due to mutations in COL2A1 or COL11A1: Why not Stickler syndrome?
por: Zhou, Lin, et al.
Publicado: (2018)

Cerulean cataract mapped to 12q13 and associated with a novel initiation codon mutation in MIP
por: Xiao, Xueshan, et al.
Publicado: (2011)

Evaluation of PRSS56 in Chinese subjects with high hyperopia or primary angle-closure glaucoma
por: Jiang, Dan, et al.
Publicado: (2013)

Non-Pharmaceutical Interventions against COVID-19 Causing a Lower Trend in Age of LHON Onset
por: Zheng, Yuxi, et al.
Publicado: (2023)

Genetic and clinical landscape of ARR3-associated MYP26: the most common cause of Mendelian early-onset high myopia with a unique inheritance
por: Wang, Yingwei, et al.
Publicado: (2023)

Clinical and linkage study on a consanguineous Chinese family with autosomal recessive high myopia
por: Yang, Zhikuan, et al.
Publicado: (2009)

Detection of Variants in 15 Genes in 87 Unrelated Chinese Patients with Leber Congenital Amaurosis
por: Li, Lin, et al.
Publicado: (2011)

The Genetic Confirmation and Clinical Characterization of LOXL3-Associated MYP28: A Common Type of Recessive Extreme High Myopia
por: Jiang, Yi, et al.
Publicado: (2023)

Genotypes and phenotypes of genes associated with achromatopsia: A reference for clinical genetic testing
por: Sun, Wenmin, et al.
Publicado: (2020)

Structural variations in a non-coding region at 1q32.1 are responsible for the NYS7 locus in two large families
por: Sun, Wenmin, et al.
Publicado: (2020)

Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular albinism
por: Fang, Shaohua, et al.
Publicado: (2008)

Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese
por: Ji, Yanli, et al.
Publicado: (2010)

A novel mutation of PAX6 in Chinese patients with new clinical features of Peters’ anomaly
por: Jia, Xiuhua, et al.
Publicado: (2010)

Identification of Genetic Defects in 33 Probands with Stargardt Disease by WES-Based Bioinformatics Gene Panel Analysis
por: Xin, Wei, et al.
Publicado: (2015)

Confirming and expanding the phenotypes of FZD5 variants: Coloboma, inferior chorioretinal hypoplasia, and high myopia
por: Jiang, Yi, et al.
Publicado: (2021)

Dominant RP in the Middle While Recessive in Both the N- and C-Terminals Due to RP1 Truncations: Confirmation, Refinement, and Questions
por: Wang, Junwen, et al.
Publicado: (2021)

Retinopathy as an initial sign of hereditary immunological diseases: report of six families and challenges in eye clinic
por: Wang, Yingwei, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_kh1h1o2b213951gblp6b98fo2g