Cargando…
Identification of 2 Potentially Relevant Gene Mutations Involved in Strabismus Using Whole-Exome Sequencing
BACKGROUND: The etiology of strabismus has a genetic component. Our study aimed to localize the candidate causative gene mutant in a Chinese family with strabismus and to describe its underlying etiology. MATERIAL/METHODS: Genomic DNA was extracted from the affected individual and his parents in a C...
Autores principales: | Min, Xiangrong, Fan, Haiying, Zhao, Guiqiu, Liu, Guixiang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395132/ https://www.ncbi.nlm.nih.gov/pubmed/28391287 http://dx.doi.org/10.12659/MSM.902823 |
Ejemplares similares
-
Identification of Possible Risk Variants of Familial Strabismus Using Exome Sequencing Analysis
por: An, Joon-Yong, et al.
Publicado: (2021) -
Identification of a novel pathogenic missense mutation in PRPF31 using whole exome sequencing: a case report
por: Bryant, Laura, et al.
Publicado: (2019) -
Somatic Mutations from Whole Exome Sequencing Analysis of the Patients with Biliary Tract Cancer
por: Yoon, Kyong-Ah, et al.
Publicado: (2018) -
Whole Exome-Sequencing of Pooled Genomic DNA Samples to Detect Quantitative Trait Loci in Esotropia and Exotropia of Strabismus in Japanese
por: Zhang, Jingjing, et al.
Publicado: (2021) -
Mutation discovery in mice by whole exome sequencing
por: Fairfield, Heather, et al.
Publicado: (2011)