Clinical characteristics of a family with early-onset Alzheimer's disease associated with a presenilin 1 mutation (M139T)

Medicina Clinica

Volumn 118, Issue 18, 2002, Pages 698-700

  Lléo, Alberto ^a   Blesa, Rafael ^a   Gendre, Jordi ^b   Catellví, Magda ^a   Molinuevo, JoséLuis ^a   Oliva, Rafael ^a  

^a HOSPITAL CLÍNIC   (Spain)

^b HOSPITAL GENERAL DE GRANOLLERS   (Spain)

Author keywords

Alzheimer's disease; Dementia; Mutation; Presenilin 1

Indexed keywords

APOLIPOPROTEIN E; METHIONINE; PRESENILIN 1; PRESENILIN 2; THREONINE; MEMBRANE PROTEIN; PSEN1 PROTEIN, HUMAN;

ADULT; ALZHEIMER DISEASE; AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BEHAVIOR DISORDER; CASE REPORT; CLINICAL FEATURE; CODON; COGNITIVE DEFECT; CONTROLLED STUDY; ENVIRONMENTAL FACTOR; FAMILIAL DISEASE; FAMILY; FAMILY HISTORY; GENE MUTATION; GENETIC ANALYSIS; GENOTYPE; HEREDITY; HUMAN; ONSET AGE; PREDICTION; SEQUENCE ANALYSIS; SINGLE STRAND CONFORMATION POLYMORPHISM; AGE; COMPARATIVE STUDY; FEMALE; GENETICS; MALE; MIDDLE AGED; MORTALITY; MUTATION; PEDIGREE; TIME;

ADULT; AGE FACTORS; ALZHEIMER DISEASE; FEMALE; HUMANS; MALE; MEMBRANE PROTEINS; MIDDLE AGED; MUTATION; PEDIGREE; PRESENILIN-1; TIME FACTORS;

EID: 0037129745     PISSN: 00257753     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0025-7753(02)72501-3     Document Type: Article

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