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Marked variation in the cardiomyopathy associated with Friedreich's ataxia
Objective—To document the cardiac phenotype associated with Friedreich's ataxia, a recessively inherited disorder characterised by spinocerebellar degeneration. Setting—Individuals with Friedreich's ataxia who accepted the invitation to participate in the study. Hypothesis—The cardiomyopat...
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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
1999
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1728941/ https://ncbi.nlm.nih.gov/pubmed/9922348 |
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