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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...

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Detaylı Bibliyografya
Asıl Yazarlar: von Kanel, Thomas, Stanke, Frauke, Weber, Melanie, Schaller, Andre, Racine, Julien, Kraemer, Richard, Chanson, Marc, Tümmler, Burkhard, Gallati, Sabina
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group 2013
Konular:
Online Erişim: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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