Early-Onset Infantile Facioscapulohumeral Muscular Dystrophy: A Timely Review

Facioscapulohumeral muscular dystrophy (FSHD)—the worldwide third most common inherited muscular dystrophy caused by the heterozygous contraction of a 3.3 kb tandem repeat (D4Z4) on a chromosome with a 4q35 haplotype—is a progressive genetic myopathy with variable onset of symptoms, distribution of...

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Detalles Bibliográficos
Autores principales: Chen, Tai-Heng, Wu, Yan-Zhang, Tseng, Yung-Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589635/
https://www.ncbi.nlm.nih.gov/pubmed/33096728
http://dx.doi.org/10.3390/ijms21207783

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589635/
https://www.ncbi.nlm.nih.gov/pubmed/33096728
http://dx.doi.org/10.3390/ijms21207783

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