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Volumn 63, Issue 11, 2004, Pages 1524-1525
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Hereditary C1q deficiency and secondary Sjögren's syndrome
b
CPRLab
(Netherlands)
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Author keywords
[No Author keywords available]
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Indexed keywords
COMPLEMENT COMPONENT C1Q;
ADOLESCENT;
ARTHRITIS;
ARTICLE;
AUTOIMMUNE DISEASE;
CASE REPORT;
COMPLEMENT DEFICIENCY;
CONSANGUINEOUS MARRIAGE;
HUMAN;
MALE;
PAROTITIS;
PRIORITY JOURNAL;
SJOEGREN SYNDROME;
SYSTEMIC LUPUS ERYTHEMATOSUS;
ADOLESCENT;
CHILD;
COMPLEMENT C1Q;
CONSANGUINITY;
HUMANS;
MALE;
POINT MUTATION;
SJOGREN'S SYNDROME;
TURKEY;
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EID: 7244251573
PISSN: 00034967
EISSN: None
Source Type: Journal
DOI: 10.1136/ard.2003.016592 Document Type: Article |
Times cited : (16)
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References (7)
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