A carregar...
Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations
BACKGROUND: Variants of several genes encoding transcription modulators, signal transduction, and structural proteins are known to cause Mendelian congenital heart disease (CHD). NKX2-5 and GATA4 were the first CHD-causing genes identified by linkage analysis in large affected families. Mutations of...
Na minha lista:
Main Authors: | , , , , , , , , , , , |
---|---|
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Blackwell Publishing Inc
2012
|
Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3370385/ https://ncbi.nlm.nih.gov/pubmed/22011241 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1747-0803.2011.00573.x |
Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|