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Article

Pigmented macules in Waardenburg syndrome type 2 due to KITLG mutation.

Pigment cell & melanoma research - 1 Sept 2017

Ogawa Yasushi, Kono Michihiro, Akiyama Masashi

Abstract excerpt

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 28504826
DOI: 10.1111/pcmr.12597

Genes

KITLG

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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Pigmented macules in Waardenburg syndrome type 2 due to KITLG mutation.PMID 28504826Read ↗

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Waardenburg syndrome type 2 in a Turkish family: implications for the importance of the pattern of fundus pigmentation.Semantic proximity Read ↗

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The genetic determination of skin pigmentation: KITLG and the KITLG/c-Kit pathway as key players in the onset of human familial pigmentary diseases.Semantic proximity Read ↗

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Identification of a novel mutation in the KITLG gene in a Chinese family with familial progressive hyper- and hypopigmentationSemantic proximity Read ↗

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