QR kȏd

Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy.

Three novel beta cardiac myosin heavy chain (MHC) gene missense mutations, Phe513Cys, Gly716Arg, and Arg719Trp, which cause familial hypertrophic cardiomyopathy (FHC) are described. One mutation in exon 15 (Phe513Cys) does not alter the charge of the encoded amino acid, and affected family members h...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Izdano u:J Clin Invest
Glavni autori: Anan, R, Greve, G, Thierfelder, L, Watkins, H, McKenna, W J, Solomon, S, Vecchio, C, Shono, H, Nakao, S, Tanaka, H
Format: Artigo
Jezik:Inglês
Izdano: American Society for Clinical Investigation 1994
Teme:
Online pristup:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC293763/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8282798/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI116957
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!