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Article

Familial progressive hyper- and hypopigmentation caused by a novel mutation in site II of the KITLG gene.

The Journal of dermatology - 1 Sept 2021

Liu Zhenfeng, Zhu Zhenlai, Luo Junjie, Yang Bin

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Identifiers

PMID: 34114687
DOI: 10.1111/1346-8138.16016

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Familial progressive hyper- and hypopigmentation caused by a novel mutation in site II of the KITLG gene.PMID 34114687Read ↗

De novo mutation in KITLG gene causes a variant of Familial Progressive Hyper- and Hypo-pigmentation (FPHH).Semantic proximity Read ↗

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

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

[Progressive familial hyperpigmentation is associated with mutations activating the KIT receptor ligand].Semantic proximity Read ↗

[Clinical phenotype and genetic analysis of a Chinese pedigree affected with familial progressive hyperpigmentation and hypopigmentation].Semantic proximity Read ↗

Familial progressive hyper- and hypopigmentation: a report on a Chinese family and evidence for genetic heterogeneity.Semantic proximity Read ↗

Familial progressive hyper- and hypopigmentation and malignancy in two families with new mutations inKITLGSemantic proximity Read ↗

KITLG mutations cause familial progressive hyper- and hypopigmentation.Semantic proximity Read ↗

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 ↗

New variant in KITLG shapes the pathogenesis of familial progressive hyper- and hypo-pigmentation.Semantic proximity Read ↗

Pigmented macules in Waardenburg syndrome type 2 due to KITLG mutation.Semantic proximity Read ↗

Lower Leg Hyperpigmentation in MYH9-Related Disorder.Semantic proximity Read ↗

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