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Article

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

Clinical genetics - 1 Jul 2008

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

Abstract excerpt

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Topics

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Share to MITF gene
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 18510545
DOI: 10.1111/j.1399-0004.2008.01010.x

Genes

MITF

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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Tietz syndrome: unique phenotype specific to mutations of MITF nuclear localization signal.PMID 18510545Read ↗

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The MITF family of transcription factors: Role in endolysosomal biogenesis, Wnt signaling, and oncogenesisSemantic proximity Read ↗

[Analysis of nuclear localization and signal function of MITF protein predisposing to Warrdenburg syndrome].Semantic proximity Read ↗

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