Clinical and molecular characterization of the potential CF disease modifier syntaxin 1A

Cystic fibrosis (CF) is caused by mutations in the CF transmembrane conductance regulator gene (CFTR). Disease severity in CF varies greatly, and sibling studies strongly indicate that genes other than CFTR modify disease outcome. Syntaxin 1A (STX1A) has been reported as a negative regulator of CFTR...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: von Kanel, Thomas, Stanke, Frauke, Weber, Melanie, Schaller, Andre, Racine, Julien, Kraemer, Richard, Chanson, Marc, Tümmler, Burkhard, Gallati, Sabina
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2013
Assuntos:
Short Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3831073/
https://ncbi.nlm.nih.gov/pubmed/23572023
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2013.57
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados