Caricamento...

Molecular basis of hypertrophic and dilated cardiomyopathy.

Hypertrophic cardiomyopathy is a heterogeneous disease with autosomal dominant Mendelian inheritance. In 1989, the 1st locus for hypertrophic cardiomyopathy was mapped to cardiac myosin genes located on chromosome 14q1. Soon, several mutations that cosegregated with inheritance of the disease were i...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Autori principali: Marian, A J, Roberts, R
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1994
Soggetti:
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC325126/
https://ncbi.nlm.nih.gov/pubmed/8180512
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !