Proline

UDP glycosyltransferase 8 ; Homo sapiens







2 Article(s)
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PMID
Title
Pub. Year
#Total Relationships
1 9141561 A novel point mutation in the insulin gene giving rise to hyperproinsulinemia. 1997 May 1
2 2722864 A novel amino acid substitution in the reactive site of a congenital variant antithrombin. Antithrombin pescara, ARG393 to pro, caused by a CGT to CCT mutation. 1989 Jun 15 1