Showing results 1 to 9 of 9
Title | Author(s) | Issue Date | |
---|---|---|---|
C4A gene deficiency in Chinese patients with systemic lupus erythematosus (SLE) Proceeding/Conference:Bi-annual Congress of the Asia Pacific League of Associations for Rheumatology, APLAR 2004 | 2004 | ||
Clinical and Molecular Characteristics of 32 Chinese Children with Wiskott-Aldrich Syndrome Proceeding/Conference:Keystone symposium on Human Immunology and Immunodeficiencies | 2009 | ||
Clinical and molecular characteristics of 35 chinese children with wiskott-aldrich syndrome Journal:Journal of Clinical Immunology | 2009 | ||
2016 | |||
Genotypic and phenotypic analyses of C4A and C4B in Chinese patients with systemic lupus erythematosus (SLE) Proceeding/Conference:Bi-annual Congress of the Asia Pacific League of Associations for Rheumatology, APLAR 2004 | 2004 | ||
2018 | |||
2021 | |||
A Missense Mutation in SLC33A1, which Encodes the Acetyl-CoA Transporter, Causes Autosomal-Dominant Spastic Paraplegia (SPG42) Journal:American Journal of Human Genetics | 2008 | ||
2014 |