Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.

Hypertrophic cardiomyopathy occurs as an autosomal dominant familial disorder or as a sporadic disease without familial involvement. While missense mutations in the beta cardiac myosin heavy chain (MHC) gene account for approximately half of all cases of familial hypertrophic cardiomyopathy, the mol...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Watkins, H, Thierfelder, L, Hwang, D S, McKenna, W, Seidman, J G, Seidman, C E
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1992
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC443222/
https://ncbi.nlm.nih.gov/pubmed/1430197
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia