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Clinical Heterogeneity Among a Three-Generation Japanese Family With D18N TREX1 Mutation for Aicardi-Goutières Syndrome / Familial Chilblain Lupus
Pediatric Rheumatology
- United Kingdom
doi 10.1186/1546-0096-9-s1-p276
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Categories
Immunology
Pediatrics
Rheumatology
Allergy
Perinatology
Child Health
Date
September 14, 2011
Authors
J Abe
R Nishikomori
K Izawa
T Awaya
T Kawai
T Yasumi
T Heike
N Hiragi
T Hiragi
Publisher
Springer Science and Business Media LLC