Population-specific spectrum of the F11 mutations in Koreans: Evidence for a founder effect

Clinical Genetics

Volumn 82, Issue 2, 2012, Pages 180-186

  Kim, J ^a   Song, J ^a   Lyu, C J ^a   Kim, Y R ^a   Oh, S H ^a   Choi, Y C ^a   Yoo, J H ^a   Choi, J R ^a   Kim, H ^a   Lee, K A ^a  

^a Yonsei University College of Medicine   (South Korea)

Author keywords

F11; Factor XI deficiency; Koreans; Mutation spectrum

Indexed keywords

BLOOD CLOTTING FACTOR 11;

ADULT; AGED; ARTICLE; BLOOD CLOTTING FACTOR 11 DEFICIENCY; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FOUNDER EFFECT; GENE MUTATION; GENETIC SCREENING; HAPLOTYPE; HUMAN; KOREA; MALE; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; SCHOOL CHILD;

ADOLESCENT; ADULT; AGED; AMINO ACID SEQUENCE; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CHILD; FACTOR XI; FACTOR XI DEFICIENCY; FEMALE; FOUNDER EFFECT; HAPLOTYPES; HUMANS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; PHENOTYPE; POLYMORPHISM, GENETIC; REPUBLIC OF KOREA; YOUNG ADULT;

EID: 84863778977     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2011.01732.x     Document Type: Article

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