Cargando…
Mutational screening of GDAP1 in dysphonia associated with Charcot-Marie-Tooth disease: clinical insights and phenotypic effects
INTRODUCTION: Mutations in GDAP1 (Ganglioside-induced differentiation-associated protein 1) gene are linked to Charcot-Marie-Tooth disease (CMT), a Heterogenous group of disorders with multiple phenotypes, characterized by peripheral nerve dysfunction that can lead to vocal cord paralysis and diaphr...
Autores principales: | Manzoor, Uzma, Ali, Awais, Ali, S. Luqman, Abdelkarem, Omneya, Kanwal, Sumaira, Alotaibi, Saqer S., Baazeem, Alaa, Baiduissenova, Aliya, Yktiyarov, Ayaz, Hajar, Azraida, Olzhabay, Abay |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651813/ https://www.ncbi.nlm.nih.gov/pubmed/37966693 http://dx.doi.org/10.1186/s43141-023-00568-9 |
Ejemplares similares
-
Clinical and Neuroimaging Features in Charcot-Marie-Tooth Patients with GDAP1 Mutations
por: Kim, Hyun Su, et al.
Publicado: (2021) -
Novel GDAP1 Mutation in a Vietnamese Family with Charcot-Marie-Tooth Disease
por: Mai, Phuong-Thao, et al.
Publicado: (2019) -
Structural insights into Charcot–Marie–Tooth disease‐linked mutations in human GDAP1
por: Sutinen, Aleksi, et al.
Publicado: (2022) -
The Gdap1 knockout mouse mechanistically links redox control to Charcot–Marie–Tooth disease
por: Niemann, Axel, et al.
Publicado: (2014) -
Mitochondria–lysosome membrane contacts are defective in GDAP1-related Charcot–Marie–Tooth disease
por: Cantarero, Lara, et al.
Publicado: (2020)