Phenotype associated with recessively inherited mutations in DNA mismatch repair (MMR) genes

Biochemical Society Transactions

Volumn 33, Issue 4, 2005, Pages 718-720

  De Vos, M ^a   Hayward, B ^a   Bonthron, D T ^a   Sheridan, E ^b  

^a UNIVERSITY OF LEEDS   (United Kingdom)

^b ST JAMES S UNIVERSITY HOSPITAL   (United Kingdom)

Author keywords

Hereditary non polyposis colon cancer (HNPCC); Mismatch repair gene (MMR gene); Recessive inheritance; Supratentorial primitive neuroectodermal tumour (SPNET)

Indexed keywords

MISMATCH REPAIR PROTEIN PMS2; PROTEIN MLH1; PROTEIN MSH2; PROTEIN MSH6;

ALLELE; AUTOSOMAL RECESSIVE DISORDER; BRAIN TUMOR; CAFE AU LAIT SPOT; CANCER SURVIVAL; CANCER SUSCEPTIBILITY; COLON CANCER; CONFERENCE PAPER; GENE DELETION; GENE INSERTION; GENE MUTATION; GENETIC ASSOCIATION; HEMATOLOGIC MALIGNANCY; HUMAN; MICROSATELLITE INSTABILITY; MISMATCH REPAIR; PHENOTYPE; PRIORITY JOURNAL; TUMOR CELL;

ADENOSINE TRIPHOSPHATASES; BASE PAIR MISMATCH; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; DNA REPAIR; DNA REPAIR ENZYMES; DNA-BINDING PROTEINS; GENES, RECESSIVE; GERM-LINE MUTATION; HUMANS; MUTATION;

EID: 23844494113     PISSN: 03005127     EISSN: None     Source Type: Journal    
DOI: 10.1042/BST0330718     Document Type: Conference Paper

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