Functional MASP2 single nucleotide polymorphism plays no role in psoriasis

British Journal of Dermatology

Volumn 152, Issue 6, 2005, Pages 1313-1315

  Stover, Cordula ^a   Barrett, S ^a   Lynch, N J ^a   Barker, J N W N ^b   Burden, D ^c   Trembath, R ^a   Schwaeble, W ^a   Veal, C ^a  

^a UNIVERSITY OF LEICESTER   (United Kingdom)

^b KING'S COLLEGE LONDON   (United Kingdom)

^c UNIVERSITY OF GLASGOW   (United Kingdom)

Author keywords

Complement; Deficiency; Lectin pathway

Indexed keywords

GENOMIC DNA; LECTIN; PROTEINASE;

ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; CHROMOSOME 1P; COHORT ANALYSIS; COMPLEMENT ACTIVATION; DISSOCIATION; GENE; GENE FREQUENCY; GENE FUNCTION; GENE LOCATION; GENETIC RISK; GENETIC SCREENING; GENETIC SUSCEPTIBILITY; GENOTYPE; HETEROZYGOTE; HUMAN; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; MASP2 GENE; MOLECULAR RECOGNITION; MUTATIONAL ANALYSIS; PARENT; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROGENY; PSORIASIS; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM; VERTICAL TRANSMISSION;

ALLELES; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MANNOSE-BINDING PROTEIN-ASSOCIATED SERINE PROTEASES; PARENTS; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; POLYMORPHISM, SINGLE NUCLEOTIDE; PSORIASIS; SERINE ENDOPEPTIDASES;

EID: 21644486204     PISSN: 00070963     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1365-2133.2005.06547.x     Document Type: Article

References (15)

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