Counselling issues in familial hypertrophic cardiomyopathy.

To illustrate the variable clinical presentations and rates of progression in familial hypertrophic cardiomyopathy (FHC), phenotypes and genotypes were compared in three FHC families with different genetic defects. In the first family, the FHC abnormality was a protein truncating mutation (Gln969X)...

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Bibliographische Detailangaben
Hauptverfasser: Yu, B, French, J A, Jeremy, R W, French, P, McTaggart, D R, Nicholson, M R, Semsarian, C, Richmond, D R, Trent, R J
Format: Artigo
Sprache:Inglês
Veröffentlicht: 1998
Schlagworte:
Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051239/
https://ncbi.nlm.nih.gov/pubmed/9541100
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