MSH2 codon 322 Gly to Asp seems not to confer an increased risk for colorectal cancer susceptibility [1]

European Journal of Cancer

Volumn 34, Issue 12, 1998, Pages 1981-

  Liu, T ^a   Stathopoulos, P ^a   Lindblom, P ^a   Rubio, C ^a   Arver, B Wasteson ^a   Iselius, L ^a   Holmberg, E ^b   Gronberg H ^b   Lindblom, A ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^b UMEÅ UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

BASE MISPAIRING; CANCER RISK; CANCER SUSCEPTIBILITY; CODON; COLORECTAL CANCER; DENATURING GRADIENT GEL ELECTROPHORESIS; DNA POLYMORPHISM; EXON; FAMILIAL CANCER; FEMALE; GENE MUTATION; GENETIC SUSCEPTIBILITY; HUMAN; LETTER; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEGREGATION ANALYSIS;

CODON; COLORECTAL NEOPLASMS; DNA-BINDING PROTEINS; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MUTATION; MUTS HOMOLOG 2 PROTEIN; PROTO-ONCOGENE PROTEINS; RISK FACTORS;

EID: 0032213520     PISSN: 09598049     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0959-8049(98)00217-2     Document Type: Letter

References (4)

1. 1. Wahlberg S, Nyström-Lahti M, Kane MF, et al. Few mutations in the hMSH2 gene in Swedish HNPCC families found by denaturing gradient gel electrophoresis. Int J Cancer 1997, 74, 134-137.
2. 2. Liu B, Parsons R, Hamilton SR, et al. hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds. Cancer Res 1994, 54, 4590-4594.
3. 3. Froggatt NJ, Joyce JA, Evans DGR, et al. MSH2 sequence variations and inherited colorectal cancer susceptibility. Eur J Cancer 1996, 32A, 178.
4. 4. Maliaka YK, Chudina AP, Belev NF, et al. CpG dinucleotides in the hMSH2 and hMLH1 genes are hotspots for HNPCC mutations. Hum Genet 1996, 97, 251-255.