ABCC8 p.Val187Pro
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PMID: 16442101
[PubMed]
Frelet A et al: "Insight in eukaryotic ABC transporter function by mutation analysis."
No.
Sentence
Comment
438
Two TMD0 mutations, A116P and V187P, abrogated the association of TMD0 and Kir6.2.
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ABCC8 p.Val187Pro 16442101:438:30
status: NEW