In vivo somatic mutations in Werner's syndrome

Human Genetics

Volumn 103, Issue 4, 1998, Pages 405-410

  Kyoizumi, Seishi ^a   Kusunoki, Yoichiro ^a   Seyama, Toshio ^a   Hatamochi, Atsushi ^b   Goto, Makoto ^c  

^a RADIATION EFFECTS RESEARCH FOUNDATION   (Japan)

^b CHIBA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c Tokyo Metropolitan Ohtsuka Hospital   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CELL RECEPTOR; GLYCOPHORIN A; HELICASE;

ADULT; ARTICLE; BLOOM SYNDROME; CELL MUTANT; CLINICAL ARTICLE; ERYTHROCYTE; FEMALE; FLOW CYTOMETRY; GENE FREQUENCY; GENE LOCUS; GENE MUTATION; HETEROZYGOSITY LOSS; HUMAN; MALE; MULTIGENE FAMILY; NORMAL HUMAN; PHENOTYPE; PRIORITY JOURNAL; SOMATIC MUTATION; T LYMPHOCYTE; WERNER SYNDROME;

ADULT; AGE FACTORS; BLOOM SYNDROME; ERYTHROCYTES; FEMALE; FLOW CYTOMETRY; GENE FREQUENCY; GLYCOPHORIN; HUMANS; LOSS OF HETEROZYGOSITY; MALE; MIDDLE AGED; MUTATION; RECEPTOR-CD3 COMPLEX, ANTIGEN, T-CELL; WERNER SYNDROME;

EID: 0031751941     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050841     Document Type: Article

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