Search and insights into novel genetic alterations leading to classical and atypical Werner Syndrome

Gerontology

Volumn 60, Issue 3, 2014, Pages 239-246

  Oshima, Junko ^a   Hisama, Fuki M ^b  

^a UNIVERSITY OF WASHINGTON   (United States)

^b UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

Author keywords

Atypical Werner syndrome; Cancer; Cardiovascular disease; Genetics; Hutchinson Gilford progeria syndrome; Mutation; Werner syndrome

Indexed keywords

LAMIN A; LAMIN C; RECQ HELICASE; WERNER SYNDROME PROTEIN; EXODEOXYRIBONUCLEASE; LMNA PROTEIN, HUMAN; WRN PROTEIN, HUMAN;

AGING; ATYPICAL WERNER SYNDROME; CHROMOSOME ABERRATION; CLASSICAL WERNER SYNDROME; CLINICAL FEATURE; COPY NUMBER VARIATION; GENE LOCUS; GENOMIC INSTABILITY; HUMAN; MISSENSE MUTATION; MOLECULAR CLONING; MOLECULAR DIAGNOSIS; PATHOGENESIS; PRIORITY JOURNAL; PROGERIA; REVIEW; WERNER SYNDROME; BULLOUS SKIN DISEASE; DISEASE REGISTRY; GENE; GENE MUTATION; GENE REARRANGEMENT; GENETIC POLYMORPHISM; LMNA GENE; NESTOR GUILLERMO PROGERIA SYNDROME; PHENOTYPE; ADULT; CHILD; FEMALE; GENETICS; MALE; MUTATION; PREMATURE AGING; REGISTER;

ADULT; AGING; AGING, PREMATURE; CHILD; CHROMOSOME ABERRATIONS; EXODEOXYRIBONUCLEASES; FEMALE; GENE REARRANGEMENT; HUMANS; LAMIN TYPE A; MALE; MUTATION; PROGERIA; RECQ HELICASES; REGISTRIES; WERNER SYNDROME;

EID: 84899464892     PISSN: 0304324X     EISSN: 14230003     Source Type: Journal    
DOI: 10.1159/000356030     Document Type: Review

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