Frameshift mutation at codon 642 of the hMLH1 gene in human endometrial cancer

Human Mutation

Volumn 8, Issue 4, 1996, Pages 394-395

  Fukushige, S ^a   Wakatsuki, S ^a   Nagase, S ^a   Horii, A ^a  

^a TOHOKU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CLINICAL ARTICLE; DNA SEQUENCE; ENDOMETRIUM CANCER; EXON; GENE DELETION; GENE MUTATION; HUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL;

EID: 0029801274     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.1380080404     Document Type: Article

References (3)

1. Han H‐J, Maruyama M, Baba S, Park J‐G, Nakamura Y (1995) Genomic structure of human mismatch repair gene, hMLH1, and its mutation analysis in patients with hereditary nonpolyposis colorectal cancer (HNPCC). Hum Mol Genet 4: 237–242.
2. Liu B, Parsons RE, Hamilton SR, Petersen GM, Lynch HT, Watson P, Markowitz S, Willson JKV, Green J, de la Chapelle A, Kinzler KW, Vogelstein B (1994) hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds. Cancer Res 54: 4590–4594.
3. Orita M, Suzuki Y, Sekiya T, Hayashi K (1989) Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction. Genomics 5: 874–879.