Vol 4: Decoding F508del Misfolding in Cystic Fibrosis.Reportar como inadecuado



 Vol 4: Decoding F508del Misfolding in Cystic Fibrosis.


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This article is from Biomolecules, volume 4.AbstractThe functional deficiency of the cystic fibrosis transmembrane conductance regulator (CFTR), a plasma membrane chloride channel, leads to the development of cystic fibrosis. The deletion of a phenylalanine at residue 508 (F508del) is the most common cause of CFTR misfolding leading to the disease.

Autor: Wang, Xiaodong Robert; Li, Chenglong

Fuente: https://archive.org/







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