Recurrent mutations and genotype-phenotype correlations in hereditary factor VII deficiency in Korea

Blood Coagulation and Fibrinolysis

Volumn 22, Issue 2, 2011, Pages 102-105

  Kwon, Min Jung ^a   Yoo, Ki Young ^b   Lee, Ki O ^c   Kim, Sun Hee ^a   Kim, Hee Jin ^a,c  

^a Sungkyunkwan University School of Medicine   (South Korea)

^b Korea Hemophilia Foundation Clinic   (South Korea)

^c Samsung Medical Center   (South Korea)

Author keywords

F7; factor VII deficiency; genotype phenotype; Korea; mutation

Indexed keywords

BLOOD CLOTTING FACTOR 7; GENOMIC DNA;

5' UNTRANSLATED REGION; ADULT; AGED; ARTICLE; BLOOD CLOTTING FACTOR 7 DEFICIENCY; BLOOD CLOTTING TEST; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; FEMALE; FRAMESHIFT MUTATION; GENE SEQUENCE; GENOTYPE PHENOTYPE CORRELATION; HETEROZYGOTE; HOMOZYGOTE; HUMAN; KOREA; MALE; MISSENSE MUTATION; MOLECULAR GENETICS; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD;

ADULT; AGED; ALLELES; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CHILD, PRESCHOOL; EXONS; FACTOR VII; FACTOR VII DEFICIENCY; FEMALE; GENETIC ASSOCIATION STUDIES; GENOTYPE; HUMANS; MALE; MIDDLE AGED; MUTATION, MISSENSE; PHENOTYPE; POINT MUTATION; POLYMERASE CHAIN REACTION; RECURRENCE; REPUBLIC OF KOREA;

EID: 79951679565     PISSN: 09575235     EISSN: None     Source Type: Journal    
DOI: 10.1097/MBC.0b013e328343641a     Document Type: Article

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