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Erratum: Mutations of the human tyrosinase gene associated with tyrosinase related oculocutaneous albinism (OCA1)
Author(s) -
Oetting W.S.,
Fryer J.P.,
King R.A.
Publication year - 1999
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/(sici)1098-1004(1999)13:1<83::aid-humu11>3.0.co;2-8
Subject(s) - tyrosinase , biology , arginine , amino acid substitution , mutation , genetics , cysteine , gene , amino acid , albinism , tryptophan , microbiology and biotechnology , biochemistry , enzyme
Patient 70, who was stated to have the mutation R77C, an arginine to cysteine amino acid substitution, was incorrectly reported. The mutation should have been R77W, an arginine to tryptophan amino acid substitution, which has been previously reported by Spritz et al. (1997). This change should also be made in Table 1 and Table 2. © 1998 Wiley‐Liss, Inc.