Multiple identification of a particular type of hereditary C1q deficiency in the Turkish population: Review of the cases and additional genetic and functional analysis

Human Genetics

Volumn 100, Issue 1, 1997, Pages 51-56

  Petry, Franz ^a   Berkel, A Izzet ^b   Loos, Michael ^a  

^a JOHANNES GUTENBERG UNIVERSITY   (Germany)

^b HACETTEPE UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT COMPONENT C1Q;

AMINO ACID SUBSTITUTION; ARTICLE; CHILD; COMPLEMENT DEFICIENCY; FEMALE; FRAMESHIFT MUTATION; HETEROZYGOTE DETECTION; HUMAN; IMMUNOGENETICS; MALE; POINT MUTATION; POLYMERASE CHAIN REACTION; POPULATION GENETICS; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SCHOOL CHILD; STOP CODON; TURKEY (REPUBLIC);

AMINO ACID SEQUENCE; BASE SEQUENCE; CHILD, PRESCHOOL; CODON, TERMINATOR; COMPLEMENT C1Q; FEMALE; GYPSIES; HETEROZYGOTE; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; SLOVAKIA; TURKEY;

EID: 0030857510     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050464     Document Type: Article

References (14)

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