Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis-Reference-Cited by-同舟云学术

Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis

Published:2009-08-19 Issue:1 Volume:18 Page:26-32
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Lin Ming-Wei,Lee Ding-Dar,Liu Tze-Tze,Lin Yong-Feng,Chen Shang-Yi,Huang Chih-Cheng,Weng Hui-Ying,Liu Yu-Fen,Tanaka Akio,Arita Ken,Lai-Cheong Joey,Palisson Francis,Chang Yun-Ting,Wong Chu-Kwan,Matsuura Isao,McGrath John A,Tsai Shih-Feng

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2009135.pdf

Reference39 articles.

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3. Tan T : Epidemiology of primary cutaneous amyloidoses in Southeast Asia. Clin Dermatol 1990; 8: 20–24.

4. Wong CK, Lin CS : Friction amyloidosis. Int J Dermatol 1988; 27: 302–307.

5. Chang YT, Wong CK, Chow KC, Tsai CH : Apoptosis in primary cutaneous amyloidosis. Br J Dermatol 1999; 40: 210–215.

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