A novel oncostatin M/interleukin‐31 receptor mutation in familial primary localized cutaneous amyloidosis
Author:
Affiliation:
1. European Cancer Stem Cell Research Institute, Cardiff School of Biosciences Cardiff University Cardiff UK
2. Molecular and Experimental Medicine, Department of Nephrology Cardiff University School of Medicine Cardiff UK
Publisher
Wiley
Subject
Dermatology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/ced.14059
Reference6 articles.
1. Clinical and genetic features of Chinese patients with lichen and macular primary localized cutaneous amyloidosis
2. Familial primary localized cutaneous amyloidosis in a Japanese family
3. Identification of an oncostatin M receptor mutation associated with familial primary cutaneous amyloidosis
4. New insight into mechanisms of pruritus from molecular studies on familial primary localized cutaneous amyloidosis
5. Primary Macular Amyloidosis: An Ultrastructural Approach to Diagnosis
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