SCOPUS 정보 검색 플랫폼

Blood Cells, Molecules, and Diseases

Volumn 33, Issue 3, 2004, Pages 344-345

The mitochondrial nt 16189 polymorphism and hereditary hemochromatosis

(4) Beutler, Ernest a Beutler, Lisa a Lee, Pauline L a Barton, James C b

a SCRIPPS RESEARCH INSTITUTE (United States)

b UNIVERSITY OF ALABAMA AT BIRMINGHAM (United States)

Author keywords

Hereditary hemochromatosis; Mitochondria; nt 16189 polymorphism

Indexed keywords

FERRITIN; MITOCHONDRIAL DNA;

ARTICLE; CLINICAL ARTICLE; DNA POLYMORPHISM; FERRITIN BLOOD LEVEL; GENE MUTATION; GENETIC VARIABILITY; GENOTYPE; HEMOCHROMATOSIS; HOMOZYGOTE; HUMAN; LIVER BIOPSY; LIVER CIRRHOSIS; MITOCHONDRION; PHENOTYPE; PRIORITY JOURNAL;

DNA MUTATIONAL ANALYSIS; DNA, MITOCHONDRIAL; FEMALE; HEMOCHROMATOSIS; HOMOZYGOTE; HUMANS; MALE; POLYMORPHISM, GENETIC; TRANSFERRIN;

EID: 7444225828 PISSN: 10799796 EISSN: None Source Type: Journal
DOI: 10.1016/j.bcmd.2004.06.006 Document Type: Article

Times cited : (11)

References (6)

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- The 16,189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.