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Article

Report of two Japanese patients with piebaldism including a novel mutation in KIT.

The Journal of dermatology - 1 Feb 2021

Nagatani Kei, Okamura Ken, Katagiri Kazumoto, Ono Ryusuke, Nishigori Chikako, Araki Yuta, Saito Toru, Hozumi Yutaka, Suzuki Tamio

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Identifiers

PMID: 33155701
DOI: 10.1111/1346-8138.15684

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Report of two Japanese patients with piebaldism including a novel mutation in KIT.PMID 33155701Read ↗

A novel mutation of KIT gene results in piebaldism in a Chinese family.Semantic proximity Read ↗

New mutations of KIT gene in two Chinese patients with piebaldism.Semantic proximity Read ↗

A novel KIT frame-shift mutation in a large Chinese family with variably severe phenotypes of piebaldism.Semantic proximity Read ↗

A novel KIT missense mutation in one Chinese family with piebaldism.Semantic proximity Read ↗

[A novel KIT gene mutation results in piebaldism].Semantic proximity Read ↗

KIT-related piebaldism in a Chinese girl.Semantic proximity Read ↗

Two children with a mild or moderate piebaldism phenotype and a father without leukoderma in a family with the same recurrent missense mutation in the kinase domain of KIT.Semantic proximity Read ↗

[A novel KIT gene mutation from a family with piebaldism in the southern part of China].Semantic proximity Read ↗

New KIT mutations in patients with piebaldism.Semantic proximity Read ↗

[Identification of a novel KIT mutation in a Chinese family affected with piebaldism].Semantic proximity Read ↗

Human piebaldism: six novel mutations of the proto-oncogene KIT.Semantic proximity Read ↗

Piebaldism with café-au-lait macules resulting from a novel mutation of KIT gene in a three-generation Chinese family.Semantic proximity Read ↗

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