I171V germline mutation in the NBS1 gene significantly increases risk of breast cancer

Breast Cancer Research and Treatment

Volumn 110, Issue 2, 2008, Pages 343-348

  Rożnowski, Krzysztof ^a   Januszkiewicz Lewandowska, Danuta ^a,b   Mosor, Maria ^b   Pernak, Monika ^b   Litwiniuk, Maria ^a   Nowak, Jerzy ^b  

^a POZNAN UNIVERSITY OF MEDICAL SCIENCES   (Poland)

^b INSTITUTE OF HUMAN GENETICS   (Poland)

Author keywords

Breast cancer; I171V mutation; NBS1 gene

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BREAST CANCER; CANCER INCIDENCE; CANCER PATIENT; CANCER RISK; CLINICAL FEATURE; CONTROLLED STUDY; EUROPE; EXON; FEMALE; GENE DELETION; GENE MUTATION; GENETIC SUSCEPTIBILITY; GERM LINE; HEMATOLOGIC MALIGNANCY; HISTOPATHOLOGY; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; NBS1 GENE; NIJMEGEN BREAKAGE SYNDROME; PRIORITY JOURNAL; PROGNOSIS; RARE DISEASE; RELATIVE; RISK FACTOR; SOLID TUMOR; TUMOR GENE;

EID: 44849105787     PISSN: 01676806     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10549-007-9734-1     Document Type: Article

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