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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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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3387016/ https://ncbi.nlm.nih.gov/pubmed/22768251 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0040173 |
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