ABCG8 p.Leu36Pro
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PMID: 17632509
[PubMed]
Buch S et al: "A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease."
No.
Sentence
Comment
48
The coding SNPs responsible for amino acid changes L36P, Q340E, M429V and G575R were monomorphic.
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ABCG8 p.Leu36Pro 17632509:48:51
status: NEW