Genetic basis of human complement C4A deficiency. Detection of a point mutation leading to nonexpression.-Reference-Cited by-同舟云学术

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Genetic basis of human complement C4A deficiency. Detection of a point mutation leading to nonexpression.

Published:1993-04-01 Issue:4 Volume:91 Page:1681-1686
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Barba G,Rittner C,Schneider P M

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Cited by 72 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The complement system and human autoimmune diseases;Journal of Autoimmunity;2022-12

2. Complement C4 Copy Number Variation is Linked to SSA/Ro and SSB/La Autoantibodies in Systemic Inflammatory Autoimmune Diseases;Arthritis & Rheumatology;2022-06-27

3. Innate Immunity: A Balance between Disease and Adaption to Stress;Biomolecules;2022-05-23

4. Human Complement C4B Allotypes and Deficiencies in Selected Cases With Autoimmune Diseases;Frontiers in Immunology;2021-10-26

5. C4;The Complement FactsBook;2018

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