Carregant...

On Genetic and Phenotypic Variability of Hypertrophic Cardiomyopathy: Nature Versus Nurture

The seminal discovery of the R403Q mutation in the beta-myosin heavy chain (MyHC) gene as a cause of hypertrophic cardiomyopathy (HCM) by Dr. Thierfelder’s group a decade ago (1) ushered in a new era in the molecular genetics of HCM. To date, over 120 mutations in 10 genes, all encoding sarcomeric p...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autor principal: Marian, Ali J.
Format: Artigo
Idioma:Inglês
Publicat: 2001
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2900847/
https://ncbi.nlm.nih.gov/pubmed/11499720
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!