Proteomic Identification of Calumenin as a G551D - CFTR Associated Protein

Cystic fibrosis (CF) is the most common lethal autosomal recessive disease in the Caucasian population. It is due to mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. To date, over 1910 mutations have been identified in the CFTR gene. Among these mutations, the CF-cau...

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Detalles Bibliográficos
Autores principales: Teng, Ling, Kerbiriou, Mathieu, Taiya, Mehdi, Le Hir, Sophie, Mignen, Olivier, Benz, Nathalie, Trouvé, Pascal, Férec, Claude
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3387016/
https://www.ncbi.nlm.nih.gov/pubmed/22768251
http://dx.doi.org/10.1371/journal.pone.0040173

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3387016/
https://www.ncbi.nlm.nih.gov/pubmed/22768251
http://dx.doi.org/10.1371/journal.pone.0040173

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