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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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| Publicado en: | Int J Mol Sci |
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| Autores principales: | , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
MDPI
2020
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7589635/ https://ncbi.nlm.nih.gov/pubmed/33096728 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21207783 |
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