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Biochemistry|June 6, 1995
Functional role of arginine-11 in the N-terminal helix of skeletal troponin C: combined mutagenesis and molecular dynamics investigationJ Gulati, A B Akella, H Su, et al.Nature Genetics|November 13, 2001
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndromeM Tartaglia, E L Mehler, R Goldberg, et al.Pageof 2