Three novel mutations in GPNMB in two pedigrees with amyloidosis cutis dyschromica-Reference-Cited by-同舟云学术

Three novel mutations in GPNMB in two pedigrees with amyloidosis cutis dyschromica

Published:2019-09 Issue:6 Volume:181 Page:1327-1329
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:Br J Dermatol

Author:

Wang J.¹,Li Y.²,Xing L.³,Zhao M.⁴,Zhang S.¹,Li Z.¹,Yao Z.²⁵,Li M.²⁵^ORCID

Affiliation:

1. Department of Dermatology Henan Provincial People's Hospital People's Hospital of Zhengzhou University School of Clinical Medicine, Henan University Zhengzhou Henan 450003 China

2. Department of Dermatology Xinhua Hospital Shanghai Jiao Tong University School of Medicine 1665, Kongjiang Road Shanghai 200092 China

3. Department of Nursing Henan Provincial People's Hospital People's Hospital of Zhengzhou University School of Clinical Medicine, Henan University Zhengzhou Henan 450003 China

4. Instrumental Analysis Center Xinhua Hospital Shanghai Jiao Tong University School of Medicine 1665, Kongjiang Road Shanghai 200092 China

5. Center for Rare Disease Shanghai China

Publisher

Wiley

Subject

Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjd.18260

Reference5 articles.

1. A clinical variety of localized cutaneous amyloidosis characterized by dyschromia (amyloidosis cutis dyschromica);Morishima T;Jpn J Dermatol B,1970

2. Amyloidosis Cutis Dyschromica, a Rare Cause of Hyperpigmentation: A New Case and Literature Review

3. Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans

4. nmb, a novel gene, is expressed in low-metastatic human melanoma cell lines and xenografts

5. Glycoprotein nonmetastatic melanoma protein b, a melanocytic cell marker, is a melanosome‐specific and proteolytically released protein

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Case Report: Amyloidosis Cutis Dyschromica: Dermoscopy and Reflectance Confocal Microscopy and Gene Mutation Analysis of a Chinese Pedigree;Frontiers in Medicine;2021-12-01

2. A homozygous Y131X GPNMB mutation in a Chinese family with amyloidosis cutis dyschromica;International Journal of Dermatology;2021-10-10

3. Amyloidosis cutis dyschromica cases caused by GPNMB mutations with different inheritance patterns;Journal of Dermatological Science;2021-10

4. Diagnosis of Primary Cutaneous Amyloidosis by Rapid 4,6-Diamidino-2-Phenylindole Staining;Dermatology;2021-08-26

5. Primary Localized Cutaneous Amyloidosis of Keratinocyte Origin: An Update with Emphasis on Atypical Clinical Variants;American Journal of Clinical Dermatology;2021-07-21