Associated Papers
KIT-related piebaldism in a Chinese girl.
Zhu L et al.
American Journal of Medical Genetics. Part A, 2020
The molecular basis of familial hypercholesterolemia in the Czech Republic: spectrum of LDLR mutations and genotype-phenotype correlations.
Tichý L et al.
Atherosclerosis, 2012
Repigmentation of leukoderma in a piebald patient associated with a novel c-KIT gene mutation, G592E, of the tyrosine kinase domain.
Arase N et al.
Journal of Dermatological Science, 2011
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