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Extension of the clinical range of facioscapulohumeral dystrophy: report of six cases
Consensual diagnostic criteria for facioscapulohumeral dystrophy (FSHD) include onset of the disease in facial or shoulder girdle muscles, facial weakness in more than 50% of affected family members, autosomal dominant inheritance in familial cases, and evidence of myopathic disease in at least one...
Tallennettuna:
| Päätekijät: | , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMJ Group
2000
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1737027/ https://ncbi.nlm.nih.gov/pubmed/10864616 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.69.1.114 |
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