Hereditary Heterozygous C2 Deficiency: Variable Clinical and Serological Manifestations Among Three Sisters-Reference-Cited by-同舟云学术

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Hereditary Heterozygous C2 Deficiency: Variable Clinical and Serological Manifestations Among Three Sisters

Published:2017-07-26 Issue:2 Volume:13 Page:
ISSN:1573-3971
Container-title:Current Rheumatology Reviews
language:en
Short-container-title:CRR

Author:

Yang Ji Wei¹,Rich Eric¹,Saint-Cyr Claire²,Bourré-Tessier Josiane³

Affiliation:

1. Rheumatology Division, Department of Medicine, Centre Hospitalier de l'Université de Montréal (CHUM), Montreal, Quebec, Canada

2. Rheumatology Division, Department of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine, Montreal, Quebec, Canada

3. Centre Hospitalier de l’Université de Montréal, Hôpital Notre-Dame, 1560 Sherbrooke Street East, Montréal, QC H2L 4M1, Canada

Publisher

Bentham Science Publishers Ltd.

Subject

Rheumatology

Cited by 4 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. Combined Heterozygous Genetic Variations in Complement C2 and C8B: An Explanation for Multidimensional Immune Imbalance?;Journal of Innate Immunity;2023

2. Proteomic characteristics of plasma and blood cells in natural aging rhesus monkeys;PROTEOMICS;2022-10-13

3. Strong Association of Combined Genetic Deficiencies in the Classical Complement Pathway With Risk of Systemic Lupus Erythematosus and Primary Sjögren's Syndrome;Arthritis & Rheumatology;2022-10-07

4. Hereditary Deficiency of the Second Component of Complement: Early Diagnosis and 21-Year Follow-Up of a Family;Medicina;2020-03-10

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