Serial Observations and Mutational Analysis of an Adoptee with Family History of Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy (HCM) is an inherited cardiac disease with an autosomal dominant mode of transmission. Comprehensive genetic screening of several genes frequently found mutated in HCM is recommended for first-degree relatives of HCM patients. Genetic testing provides the means to identif...

Descripción completa

Detalles Bibliográficos
Autores principales: Harris, Bronwyn, Pfotenhauer, Jean P., Silverstein, Cheri A., Markham, Larry W., Schafer, Kim, Exil, Vernat J., Hong, Charles C.
Formato: Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2838361/
https://www.ncbi.nlm.nih.gov/pubmed/20309391
http://dx.doi.org/10.4061/2010/697269

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2838361/
https://www.ncbi.nlm.nih.gov/pubmed/20309391
http://dx.doi.org/10.4061/2010/697269

Ejemplares similares