Associated Papers
Familial Amyloidosis Cutis Dyschromica with GPNMB mutation: A Case Report and Literature Review.
Untaaveesup S et al.
Acta Dermato-venereologica, 2025
A homozygous Y131X GPNMB mutation in a Chinese family with amyloidosis cutis dyschromica.
Wang X et al.
International Journal of Dermatology, 2022
Three novel mutations in GPNMB in two pedigrees with amyloidosis cutis dyschromica.
Wang J et al.
The British Journal of Dermatology, 2019
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