KITLG Mutations Cause Familial Progressive Hyper- and Hypopigmentation
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference30 articles.
1. Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype;Brems;Nat Genet,2007
2. Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family;Bukhari;J Eur Acad Dermatol Venereol,2006
3. Getting a first clue about SPRED functions;Bundschu;Bioessays,2007
4. Somatic mutation analysis in NF1 cafe au lait spots reveals two NF1 hits in the melanocytes;De Schepper;J Invest Dermatol,2008
5. Expression and subcellular localization of Spred proteins in mouse and human tissues;Engelhardt;Histochem Cell Biol,2004
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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. A novel KITLG mutation causes familial progressive hyperpigmentation and hypopigmentation with multiple café-au-lait macules;Indian Journal of Dermatology, Venereology and Leprology;2024-07-01
3. Temporal Single Cell Analysis of Leukemia Microenvironment Identifies Taurine-Taurine Transporter Axis as a Key Regulator of Myeloid Leukemia;2024-05-14
4. Therapeutic modulation of KIT ligand in melanocytic disorders with implications for mast cell diseases;Experimental Dermatology;2024-05
5. Genetic Disorders of Pigmentation;Rook's Textbook of Dermatology;2024-03-19
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