Tietz syndrome: Unique phenotype specific to mutations of MITF nuclear localization signal

T. Izumi, A. Kohta, Y. Kimura, S. Ishida, T. Takahashi, A. Ishiko, Kenjiro Kosaki

Research output: Contribution to journalLetter

21 Citations (Scopus)
Original languageEnglish
Pages (from-to)93-95
Number of pages3
JournalClinical Genetics
Volume74
Issue number1
DOIs
Publication statusPublished - 2008 Jul 1

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this