Molecular basis and inheritance patterns of amyloidosis cutis dyschromica-Reference-Cited by-同舟云学术

Molecular basis and inheritance patterns of amyloidosis cutis dyschromica

Published:2020-02-25 Issue:5 Volume:45 Page:650-653
ISSN:0307-6938
Container-title:Clinical and Experimental Dermatology
language:en
Short-container-title:Clin Exp Dermatol

Author:

Chiu F. P. C.¹^ORCID,Wessagowit V.²,Cakmak M. F.¹,Doolan B. J.¹^ORCID,Kootiratrakarn T.²,Chaowalit P.²,Bunnag T.²,Simpson M. A.³,McGrath J. A.¹^ORCID,Onoufriadis A.¹^ORCID

Affiliation:

1. St John’s Institute of Dermatology School of Basic and Medical Biosciences King’s College London London UK

2. Department of Medical and Molecular Genetics School of Basic and Medical Biosciences King’s College London London UK

3. The Institute of Dermatology Department of Medical Services Ministry of Public Health Thailand

Publisher

Wiley

Subject

Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ced.14183

Reference6 articles.

1. Familial Primary Localized Cutaneous Amyloidosis Results from Either Dominant or Recessive Mutations in OSMR

2. Amyloidosis cutis dyschromica in two siblings and review of the epidemiology, clinical features and management in 48 cases

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

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

5. Semidominant GPNMB Mutations in Amyloidosis Cutis Dyschromica

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

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

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