Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

Nature

Volumn 376, Issue 6543, 1995, Pages 775-778

  Rogaev, E I ^a,b   Sherrington, R ^a,b   Rogaeva, E A ^a,b   Levesque, G ^a,b   Ikeda, M ^a,b   Liang, Y ^a,b   Chi, H ^a,b   Lin, C ^a,b   Holman, K ^a,b   Tsuda, T ^a,b   Mar, L ^c   Sorbi, S ^d   Nacmias, B ^d   Piacentini, S ^d   Amaducci, L ^d   Chumakov, I ^e   Cohen, D ^e   Lannfelt, L ^f   Fraser, P E ^a,b   Rommens, J M ^c   George Hyslop, P H St ^a   more..

^a UNIVERSITY OF TORONTO   (Canada)

^b TORONTO GENERAL HOSPITAL   (Canada)

^c HOSPITAL FOR SICK CHILDREN   (Canada)

^d UNIVERSITY OF FLORENCE   (Italy)

^e Ctr d'Etud du Polymorphisme Humain 27 Rue Juliette Dodu 75010   (France)

^f KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN;

ALZHEIMER DISEASE; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ARTICLE; CHROMOSOME 1; CHROMOSOME 14Q; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE PREDISPOSITION; GENE LOCATION; GENE MUTATION; HUMAN; HUMAN CELL; HUMAN TISSUE; MOLECULAR CLONING; MULTIGENE FAMILY; NUCLEOTIDE SEQUENCE; ONSET AGE; OPEN READING FRAME; PRIORITY JOURNAL; PROTEIN DOMAIN;

ALZHEIMER DISEASE; AMINO ACID SEQUENCE; BASE SEQUENCE; CHROMOSOMES, HUMAN, PAIR 1; DNA; HUMAN; MEMBRANE PROTEINS; MOLECULAR SEQUENCE DATA; MUTATION; SEQUENCE HOMOLOGY, AMINO ACID; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0029101491     PISSN: 00280836     EISSN: None     Source Type: Journal    
DOI: 10.1038/376775a0     Document Type: Article

References (9)

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