Cargando…
GJB1 Gene Analysis in Two Extended Families with X-Linked Charcot-Marie-Tooth Disease
X-linked Charcot-Marie-Tooth (CMT) disease type I (CMTX1) is the second most frequent type of CMT disease caused by pathogenic variants in the GJB1 gene. We described 2 extended cases (families) with CMTX1 with identified pathogenic variants – p.Val139Met and p.Arg215Trp. In both the families, neuro...
Autores principales: | Kovale, Sabine, Terauda, Ruta, Millere, Elina, Taurina, Gita, Murmane, Daiga, Isakova, Jekaterina, Kenina, Viktorija, Gailite, Linda |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299378/ https://www.ncbi.nlm.nih.gov/pubmed/34326750 http://dx.doi.org/10.1159/000515170 |
Ejemplares similares
-
Clinical Phenotyping and Biomarkers in Spinal and Bulbar Muscular Atrophy
por: Millere, Elina, et al.
Publicado: (2021) -
Genetic analysis and natural history of Charcot-Marie-Tooth disease CMTX1 due to GJB1 variants
por: Record, Christopher J, et al.
Publicado: (2023) -
A novel splicing mutation in 5'UTR of GJB1 causes X‐linked Charcot—Marie–tooth disease
por: Li, MeiYi, et al.
Publicado: (2022) -
Rocuronium-induced respiratory paralysis refractory to sugammadex in Charcot-Marie-Tooth disease
por: Hiramatsu, Sakiko, et al.
Publicado: (2021) -
Overview of Neuromuscular Disorder Molecular Diagnostic Experience for the Population of Latvia
por: Lace, Baiba, et al.
Publicado: (2022)