Associated Papers
Familial Amyloidosis Cutis Dyschromica with GPNMB mutation: A Case Report and Literature Review.
Untaaveesup S et al.
Acta Dermato-venereologica, 2025
T-cell acute lymphoblastic leukemia with a rare chromosomal translocation presenting as leukemia cutis.
Arora P et al.
International Journal of Dermatology, 2022
A homozygous Y131X GPNMB mutation in a Chinese family with amyloidosis cutis dyschromica.
Wang X et al.
International Journal of Dermatology, 2022
Editorial: Genetic mutations in cutaneous malignancies and non-cutaneous diseases.
Paolino G et al.
Frontiers in Medicine, 2022
Amyloidosis cutis dyschromica cases caused by GPNMB mutations with different inheritance patterns.
Qin W et al.
Journal of Dermatological Science, 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
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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