Mosaicism for a KITLG Mutation in Linear and Whorled Nevoid Hypermelanosis
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference16 articles.
1. KITLG mutations cause familial progressive hyper- and hypopigmentation;Amyere;J Invest Dermatol,2011
2. Conditional deletion of Kit in melanocytes: white spotting phenotype is cell autonomous;Aoki;J Invest Dermatol,2015
3. Analysis of 36 cases of Blaschkoid dyspigmentation: reading between the lines of Blaschko;Cohen;Pediatr Dermatol,2014
4. Familial progressive hyper- and hypopigmentation and malignancy in two families with new mutations in KITLG;Cuell;Clin Exp Dermatol,2015
5. The paracrine role of stem cell factor/c-kit signaling in the activation of human melanocytes in ultraviolet-B-induced pigmentation;Hachiya;J Invest Dermatol,2001
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1. A case of familial progressive hyperpigmentation with or without hypopigmentation presenting with hypopigmented striae along the lines of Blaschko;The Journal of Dermatology;2024-09-13
2. Therapeutic modulation of KIT ligand in melanocytic disorders with implications for mast cell diseases;Experimental Dermatology;2024-05
3. Genetic Disorders of Pigmentation;Rook's Textbook of Dermatology;2024-03-19
4. Reflectance confocal microscopy‐assisted diagnosis of lichen planus pigmentosus distributed along multiple unilateral Blaschko's lines in a child: A case report;Australasian Journal of Dermatology;2023-01-30
5. Nevi;Mosaicism in Human Skin;2022-11-24
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