Missense mutations in the chromosome 14 familial Alzheimer's disease presenilin 1 gene

Human Mutation

Volumn 11, Issue 3, 1998, Pages 216-221

  Poorkaj, Parvoneh ^a   Sharma, Vikram ^b   Anderson, Leojean ^a   Nemens, Ellen ^a   Alonso, Ma Elias ^c   Orr, Harry ^d   White, June ^e   Heston, Leonard ^a   Bird, Thomas D ^a,f   Schellenberg, Gerard D ^a,f,g  

^a UNIVERSITY OF WASHINGTON   (United States)

^b Ingenex Inc   (United States)

^c NATIONAL INSTITUTE OF NEUROLOGY AND NEUROSURGERY   (Mexico)

^d UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

^e UNIVERSITY OF MINNESOTA   (United States)

^f VA PUGET SOUND HEALTH CARE SYSTEM   (United States)

^g GRECC   (United States)

Author keywords

Alzheimer's disease; Dementia; Mutations; Presenilin 1; Presenilin 2; S182; STM2

Indexed keywords

PRESENILIN 1;

ALZHEIMER DISEASE; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 14; HUMAN; HUMAN CELL; MISSENSE MUTATION; MUTATION RATE; ONSET AGE; PATHOGENESIS; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

ADULT; AGE OF ONSET; AGED; AGED, 80 AND OVER; ALZHEIMER DISEASE; CHROMOSOMES, HUMAN, PAIR 14; DNA MUTATIONAL ANALYSIS; FEMALE; GENES, DOMINANT; GENETIC SCREENING; HUMANS; MALE; MEMBRANE PROTEINS; MIDDLE AGED; POINT MUTATION; PRESENILIN-1;

EID: 6844258883     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(1998)11:3<216::AID-HUMU6>3.0.CO;2-F     Document Type: Article

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