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...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Hauptverfasser: von Kanel, Thomas, Stanke, Frauke, Weber, Melanie, Schaller, Andre, Racine, Julien, Kraemer, Richard, Chanson, Marc, Tümmler, Burkhard, Gallati, Sabina
Format: Artigo
Sprache:Inglês
Veröffentlicht: Nature Publishing Group 2013
Schlagworte:
Short Report
Online Zugang: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
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