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P gene mutations associated with oculocutaneous albinism type II (OCA2)
Author(s) -
Oetting William S.,
Garrett Sarah Savage,
Brott Marcia,
King Richard A.
Publication year - 2005
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/humu.9318
Subject(s) - biology , oculocutaneous albinism , genetics , frameshift mutation , missense mutation , mutation , albinism , nonsense mutation , gene , microbiology and biotechnology