ABCC7 p.Gln237Ala
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PMID: 15776432
[PubMed]
Clain J et al: "Misprocessing of the CFTR protein leads to mild cystic fibrosis phenotype."
No.
Sentence
Comment
201
To test this possibility, these residues were replaced one at a time by Ala (p.T122A, p.C128A, p.S135A, p.C225A, and p.Q237A) together with the p.L206W mutation, and the processing at steady-state was examined.
X
ABCC7 p.Gln237Ala 15776432:201:119
status: NEW