Familial primary localized cutaneous amyloidosis in a Japanese family-Reference-Cited by-同舟云学术

Familial primary localized cutaneous amyloidosis in a Japanese family

Published:2016-08 Issue:2 Volume:83 Page:162-164
ISSN:0923-1811
Container-title:Journal of Dermatological Science
language:en
Short-container-title:Journal of Dermatological Science

Author:

Ueo Daisuke,Utani Atsushi,Okubo Yumi,Yozaki Mariko,Mine Yoshiko,Anan Takashi,Nishida Haruto,Takahashi Daisuke,Sakai Takashi,Hatano Yutaka,Fujiwara Sakuhei

Publisher

Elsevier BV

Subject

Dermatology,Molecular Biology,Biochemistry

Reference10 articles.

1. Oncostatin M receptor-β mutations underlie familial primary localized cutaneous amyloidosis;Arita;Am. J. Hum. Genet.,2008

2. A novel OSMR mutation in familial primary localized cutaneous amyloidosis in a Japanese family;Arita;J. Dermatol. Sci.,2009

3. Identification of an oncostatin M receptor mutation associated with familial primary cutaneous amyloidosis;Babilas;Br. J. Dermatol.,2009

4. The molecular skin pathology of familial primary localized cutaneous amyloidosis;Tanaka;Exp. Dermatol.,2010

5. Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis;Lin;Eur. J. Hum. Genet.,2010

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