Prevalence and disease progression of genetically-confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) in China between 2001 and 2020: a nationwide population-based study

BACKGROUND: Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a rare disease, which is often underdiagnosed due to its heterogeneous presentations and complex molecular genetic basis, leading to a lack of population-based epidemiology data, especially of prevalence and disease progression. ME...

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Detalles Bibliográficos
Autores principales: Wang, Zhiqiang, Qiu, Liangliang, Lin, Minting, Chen, Long, Zheng, Fuze, Lin, Lin, Lin, Feng, Ye, Zhixian, Lin, Xiaodan, He, Junjie, Wang, Lili, Lin, Xin, He, Qifang, Chen, Wanjin, Lin, Yi, Fu, Ying, Wang, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671729/
https://www.ncbi.nlm.nih.gov/pubmed/35024656
http://dx.doi.org/10.1016/j.lanwpc.2021.100323

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671729/
https://www.ncbi.nlm.nih.gov/pubmed/35024656
http://dx.doi.org/10.1016/j.lanwpc.2021.100323

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