Associated Papers
Functional Domains and Evolutionary History of the PMEL and GPNMB Family Proteins.
Chrystal PW et al.
Molecules (basel, Switzerland), 2021
Case Report: Amyloidosis Cutis Dyschromica: Dermoscopy and Reflectance Confocal Microscopy and Gene Mutation Analysis of a Chinese Pedigree.
Wang H et al.
Frontiers in Medicine, 2021
Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.
Yang CF et al.
American Journal of Human Genetics, 2018
Amyloidosis cutis dyschromica caused by compound heterozygous GPNMB mutations in a Chinese pedigree.
Zhong CJ et al.
Anais Brasileiros De Dermatologia, 0
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