Hereditary C1q deficiency: A new family with C1qA deficiency

Turkish Journal of Pediatrics

Volumn 52, Issue 2, 2010, Pages 184-186

  Sun Tan, Çaǧman ^a   Turul Özgür, Tuba ^a   Kilinç, Gamze ^a   Topaloǧlu, Rezan ^a   Gököz, Özay ^a   Ersoy Evans, Sibel ^a   Sanal, Özden ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

Author keywords

C1q deficiency; C1qA chain; Infection; Systemic lupus erythematosus

Indexed keywords

ANTINUCLEAR ANTIBODY; COMPLEMENT COMPONENT C1Q;

ANTIBODY DETECTION; ANTIBODY TITER; ARTICLE; CASE REPORT; CLINICAL FEATURE; COMPLEMENT COMPONENT C1Q DEFICIENCY; COMPLEMENT DEFICIENCY; DESQUAMATION; DYSKERATOSIS; ERYTHEMA; EXON; GENE MUTATION; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; HYPERKERATOSIS; HYPOPIGMENTATION; INFANT; LYMPHADENOPATHY; MALE; PHYSICAL EXAMINATION; RASH; SKIN ATROPHY; SKIN BIOPSY; STOP CODON; SYSTEMIC LUPUS ERYTHEMATOSUS; BLOOD; BLOOD PROTEIN DISORDER; CONSANGUINITY; DISEASE PREDISPOSITION; GENETICS; PEDIGREE; POINT MUTATION; PRESCHOOL CHILD; SKIN DISEASE;

BLOOD PROTEIN DISORDERS; CHILD, PRESCHOOL; COMPLEMENT C1Q; CONSANGUINITY; DISEASE SUSCEPTIBILITY; FACIAL DERMATOSES; HUMANS; LUPUS ERYTHEMATOSUS, SYSTEMIC; MALE; PEDIGREE; POINT MUTATION;

EID: 77955502394     PISSN: 00414301     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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