Variant chronic infantile neurologic, cutaneous, articular syndrome due to a mutation within the leucine-rich repeat domain of CIAS1.

Arthritis and rheumatism ·Vol. 50 ·No. 8 ·2004-08-00 ·Pages 2719-20

Frenkel J, van Kempen MJ, Kuis W, van Amstel HK

Abstract

暂无摘要

MeSH Terms

Adolescent Carrier Proteins/genetics Humans Male Mutation NLR Family, Pyrin Domain-Containing 3 Protein Nervous System Diseases/genetics Skin Diseases/genetics Syndrome Vascular Diseases/genetics

Chemicals

Carrier Proteins NLR Family, Pyrin Domain-Containing 3 Protein NLRP3 protein, human

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Frenkel Joost

van Kempen Marjan J A

Kuis Wietse

van Amstel Hans Kristian Ploos

Article Info

Journal

Arthritis and rheumatism

Abbr.

Arthritis Rheum

ISSN

0004-3591

DOI

10.1002/art.20295

Published

2004-08-00

Pages

2719-20

Language

English

Region

United States

NLM ID

0370605

Subset

Corrections

CommentIn

PMID: 16871551

External Links

PubMed source DOI: 10.1002/art.20295 View journal details

Analysis Services

Variant chronic infantile neurologic, cutaneous, articular syndrome due to a mutation within the leucine-rich repeat domain of CIAS1.

Contact

WeChat Official Account