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Tietz syndrome: unique phenotype specific to mutations of MITF nuclear localization signal
Author(s) -
Izumi K,
Kohta T,
Kimura Y,
Ishida S,
Takahashi T,
Ishiko A,
Kosaki K
Publication year - 2008
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2008.01010.x
Subject(s) - library science , artificial intelligence , psychology , computer science