Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Repigmentation of leukoderma in a piebald patient associated with a novel c-KIT gene mutation, G592E, of the tyrosine kinase domain.

Journal of dermatological science - 1 Nov 2011

Arase Noriko, Wataya-Kaneda Mari, Oiso Naoki, Tanemura Atsushi, Kawada Akira, Suzuki Tamio, Katayama Ichiro

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child, Preschool
Share to KIT gene
Share to Hypopigmentation
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Piebaldism

Share to Proto-Oncogene Proteins c-kit

Share to Skin Pigmentation

Source

Identifiers

PMID: 21925843
DOI: 10.1016/j.jdermsci.2011.08.006

Genes

KIT

Variants

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Repigmentation of leukoderma in a piebald patient associated with a novel c-KIT gene mutation, G592E, of the tyrosine kinase domain.PMID 21925843Read ↗

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 ↗

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

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

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

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

A novel KIT mutation results in piebaldism with progressive depigmentation.Semantic proximity Read ↗

Mutations in the ligand-binding domain of the kit receptor: an uncommon site in human piebaldism.Semantic proximity Read ↗

Piebald trait: implication of kit mutation on in vitro melanocyte survival and on the clinical application of cultured epidermal autografts.Semantic proximity Read ↗

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

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

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

Human piebald trait resulting from a dominant negative mutant allele of the c-kit membrane receptor gene.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.