Long-term follow-up of R403W(MYH7) and R92W(TNNT2) HCM families: mutations determine left ventricular dimensions but not wall thickness during disease progression

BACKGROUND: The clinical profile and prognosis of patients with hypertrophic cardiomyopathy, a primary cardiac muscle disease caused mostly by mutations in sarcomeric protein-encoding genes, have been linked to particular disease-causing mutations in the past. However, such associations are often ba...

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Detalles Bibliográficos
Autores principales: Revera, Miriam, Van Der Merwe, Lize, Heradien, Marshall, Goosen, Althea, Brink, Paul A, Corfield, Valerie A, Moolman-Smook, Johanna C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Clinics Cardive Publishing 2007
Materias:
Cardiovascular Topics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213759/
https://www.ncbi.nlm.nih.gov/pubmed/17612745

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213759/
https://www.ncbi.nlm.nih.gov/pubmed/17612745

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