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 journalLetterpeer-review

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

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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