Single nucleotide polymorphism spectra in newborns and centenarians: Identification of genes coding for rise of mortal disease

Gene

Volumn 223, Issue 1-2, 1998, Pages 381-391

  Tomita Mitchell, Aoy ^a   Muniappan, Brindha P ^a   Herrero Jimenez, Pablo ^a   Zarbl, Helmut ^b   Thilly, William G ^a  

^a Center for Environmental Health Sciences   (United States)

^b Fred Hutchinson Cancer Research Center   (United States)

Author keywords

CDCE; Centenarians; Hotspots; Monogenic; Multigenic; Mutations; Polygenic inheritance

Indexed keywords

AGED; AGING; CONFERENCE PAPER; CONTROLLED STUDY; GENE FREQUENCY; GENE INACTIVATION; GENE MUTATION; GENETIC POLYMORPHISM; GENOME; HUMAN; HUMAN CELL; MORTALITY; NEWBORN; NEWBORN PERIOD; NUCLEOTIDE SEQUENCE; PANCREAS CANCER; POINT MUTATION; PRIORITY JOURNAL; RISK FACTOR; SOMATIC MUTATION;

AGE FACTORS; AGED; AGED, 80 AND OVER; BLOOD SPECIMEN COLLECTION; ELECTROPHORESIS, CAPILLARY; FEMALE; GENETIC DISEASES, INBORN; GENETIC PREDISPOSITION TO DISEASE; GENETICS, POPULATION; HUMANS; INFANT, NEWBORN; MALE; MODELS, BIOLOGICAL; MODELS, GENETIC; MUTATION; PANCREATIC NEOPLASMS; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; RISK FACTORS; UNITED STATES;

EID: 0032570015     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1119(98)00408-9     Document Type: Conference Paper

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