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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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Hlavní autoři: Dutka, D, Donnelly, J, Nihoyannopoulos, P, Oakley, C, Nunez, D
Médium: Artigo
Jazyk:Inglês
Vydáno: 1999
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1728941/
https://ncbi.nlm.nih.gov/pubmed/9922348
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