SCOPUS 정보 검색 플랫폼

Blood

Volumn 122, Issue 4, 2013, Pages 471-473

VWF sequence variants: A data goldmine

(1) Goodeve, Anne C a,b

a UNIVERSITY OF SHEFFIELD (United Kingdom)

b SHEFFIELD CHILDREN'S NHS FOUNDATION TRUST (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 8; RISTOCETIN; VON WILLEBRAND FACTOR;

AFRICAN AMERICAN; ALLELE; ARTICLE; BLOOD CLOTTING TEST; ENDOTHELIAL DYSFUNCTION; EUROPE; GENE FREQUENCY; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC VARIABILITY; HUMAN; MISSENSE MUTATION; PATHOPHYSIOLOGY; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; SYMPTOM; VON WILLEBRAND DISEASE; FEMALE; GENETICS; MALE; NOTE;

AFRICAN AMERICANS; FACTOR VIII; FEMALE; HUMANS; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; VON WILLEBRAND FACTOR;

EID: 84886898848 PISSN: 00064971 EISSN: 15280020 Source Type: Journal
DOI: 10.1182/blood-2013-06-506147 Document Type: Article

Times cited : (3)

References (9)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.