Molecular, genetic and epidemiologic studies on selective complete C1q deficiency in Turkey

Immunobiology

Volumn 201, Issue 3-4, 2000, Pages 347-355

  Berkel, Ahmet Izzet ^a   Birben, Esra ^a   Öner, Cihan ^a   Öner, Reyhan ^a   Loos, Michael ^b   Petry, Franz ^b  

^a HACETTEPE UNIVERSITY   (Turkey)

^b JOHANNES GUTENBERG UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT COMPONENT C1Q;

ADOLESCENT; ADULT; ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; CHILD; CLINICAL ARTICLE; COMPLEMENT DISORDER; CYPRUS; EXON; FAMILIAL DISEASE; FEMALE; GENE FREQUENCY; GENE MAPPING; GENE MUTATION; HUMAN; LUPUS ERYTHEMATOSUS; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SLOVAKIA; STOP CODON; TURKEY (REPUBLIC);

EID: 0033954028     PISSN: 01712985     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0171-2985(00)80089-3     Document Type: Article

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