Molecular basis of a new type of C1q-deficiency associated with a non- functional low molecular weight (LMW) C1q: Parallels and differences to other known genetic C1q-defects

Immunopharmacology

Volumn 38, Issue 1-2, 1997, Pages 189-201

  Petry, Franz ^a   Hauptmann, Georges ^b   Goetz, Joèlle ^b   Grosshans, Edouard ^b   Loos, Michael ^a  

^a JOHANNES GUTENBERG UNIVERSITY   (Germany)

^b UNIVERSITY HOSPITAL OF STRASBOURG   (France)

Author keywords

C1q deficiency; Mutation; Sequence analysis; Systemic lupus erythematosus

Indexed keywords

ASPARTIC ACID; COLLAGEN; COMPLEMENT COMPONENT C1Q; DNA; GLYCINE;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CLINICAL ARTICLE; COMPLEMENT DEFICIENCY; DNA SEQUENCE; FAMILY STUDY; FEMALE; GENETIC DISORDER; HUMAN; MALE; MOLECULAR WEIGHT; MOROCCO; POINT MUTATION; PRIORITY JOURNAL; SYSTEMIC LUPUS ERYTHEMATOSUS;

ADOLESCENT; ADULT; CHILD; COLLAGEN; COMPLEMENT C1Q; COMPLEMENT HEMOLYTIC ACTIVITY ASSAY; DNA; EXONS; FEMALE; HUMANS; IMMUNODIFFUSION; LUPUS ERYTHEMATOSUS, SYSTEMIC; MALE; MOLECULAR WEIGHT; MOROCCO; POINT MUTATION; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS;

EID: 0031442782     PISSN: 01623109     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0162-3109(97)00065-9     Document Type: Article

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