Exclusion of catalytic and regulatory subunits of cAMP-dependent protein kinase as candidate genes for the defect causing cystic fibrosis.

Cystic fibrosis (CF) is a common autosomal recessive disease with significant morbidity and mortality. Defects in cAMP control mechanisms are implicated in the pathophysiology of the disease. The mutation causing CF has been localized to chromosome 7q22-7q31.1. We have used (1) somatic-cell hybrids...

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Detaylı Bibliyografya
Asıl Yazarlar: Scambler, P, Oyen, O, Wainwright, B, Farrall, M, Law, H Y, Estivill, X, Sandberg, M, Williamson, R, Jahnsen, T
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1987
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1684338/
https://ncbi.nlm.nih.gov/pubmed/3479018
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