Cargando…
The identification of a novel splicing mutation in the DMD gene of a Chinese family
The proband is a five‐year‐old boy diagnosed with Duchenne muscular dystrophy (DMD) by clinical manifestations and laboratory examination, but clinical phenotype of his parents is normal. In the study, his mother had a second pregnancy, and they went to obstetrics for genetic counseling to make info...
Autores principales: | Liu, Wanlu, Shi, Xinwei, Li, Yuqi, Qiao, Fuyuan, Wu, Yuanyuan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8659554/ https://www.ncbi.nlm.nih.gov/pubmed/34938549 http://dx.doi.org/10.1002/ccr3.5166 |
Ejemplares similares
-
The identification of a novel frameshift insertion mutation in the
EXT1
gene in a Chinese family with hereditary multiple exostoses
por: Liu, Wanlu, et al.
Publicado: (2022) -
Genetic testing and diagnostic strategies of fetal skeletal dysplasia: a preliminary study in Wuhan, China
por: Liu, Wanlu, et al.
Publicado: (2023) -
Identification of Two Novel Variants of the DMD Gene in Chinese Families with Duchenne Muscular Dystrophy
por: Wu, Jiangfen, et al.
Publicado: (2023) -
Splicing Characteristics of Dystrophin Pseudoexons and Identification of a Novel Pathogenic Intronic Variant in the DMD Gene
por: Xie, Zhiying, et al.
Publicado: (2020) -
A novel DMD splicing mutation found in a family responsible for X-linked dilated cardiomyopathy with hyper-CKemia
por: Tang, Jin, et al.
Publicado: (2018)