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Volumn 208, Issue 3, 1996, Pages 195-198

Three different mutations of presenilin 1 gene in early-onset Alzheimer' s disease families

Author keywords

Alzheimer's disease; Dominant inheritance; Missense mutation; Penetrance; Presenilin 1; Transmembrane domain

Indexed keywords

PRESENILIN; UNCLASSIFIED DRUG;

EID: 0029968528     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/0304-3940(96)12587-8     Document Type: Article
Times cited : (59)

References (17)
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    • Alzheimer's Disease Collaborative Group, The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families, Nature Genet., 11 (1995) 219-222.
    • (1995) Nature Genet. , vol.11 , pp. 219-222
  • 5
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    • A sodium channel defect in hyperkalemic periodic paralysis: Potassium-induced failure of inactivation
    • Cannon, S.C., Brown, Jr., R.H. and Corey, D.P., A sodium channel defect in hyperkalemic periodic paralysis: potassium-induced failure of inactivation, Neuron, 6 (1991) 619-626.
    • (1991) Neuron , vol.6 , pp. 619-626
    • Cannon, S.C.1    Brown R.H., Jr.2    Corey, D.P.3
  • 9
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    • Facilitation of lin-12-mediated signalling by sel-12, a caenorhabiditis elegans S182 Alzheimer's disease gene
    • Levitan, D. and Greenwald, J., Facilitation of lin-12-mediated signalling by sel-12, a Caenorhabiditis elegans S182 Alzheimer's disease gene, Nature, 377 (1995) 351-354.
    • (1995) Nature , vol.377 , pp. 351-354
    • Levitan, D.1    Greenwald, J.2
  • 16
    • 0029671219 scopus 로고    scopus 로고
    • 2+-binding protein ALG-2 and Alzheimer's disease gene ALG-3
    • 2+-binding protein ALG-2 and Alzheimer's disease gene ALG-3, Science, 271 (1996) 521-525.
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    • Vito, P.1    Lacaná, E.2    D'Adamo, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.