Delineation of additional genetic bases for C8β deficiency: Prevalence of null alleles and predominance of C→T transition in their genesis

Journal of Immunology

Volumn 155, Issue 10, 1995, Pages 5022-5028

  Saucedo, L ^a   Ackermann, L ^a   Platonov, A E ^a   Gewurz, A ^a   Rakita, R M ^a   Densen, P ^a  

^a Department of Internal Medicine ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT COMPONENT C8B;

ARTICLE; CLINICAL ARTICLE; COMPLEMENT DEFICIENCY; EXON; FEMALE; GENE LOCATION; GENE MUTATION; GENETIC SCREENING; HUMAN; MALE; NUCLEIC ACID BASE SUBSTITUTION; PRIORITY JOURNAL; SEQUENCE ANALYSIS; STOP CODON; UNITED STATES; USSR;

ALLELES; BASE SEQUENCE; COMPLEMENT 8; DNA PRIMERS; FAMILY; FEMALE; HUMAN; MALE; MOLECULAR SEQUENCE DATA; POINT MUTATION; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, NON-P.H.S.; UNITED STATES; USSR;

EID: 0028793204     PISSN: 00221767     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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