A novel presenilin 1 mutation (Ser169del) in a Chinese family with early-onset Alzheimer's disease

Neuroscience Letters

Volumn 468, Issue 1, 2010, Pages 34-37

  Guo, Jifeng ^a,c   Wei, Jiaohua ^a   Liao, Shusheng ^a   Wang, Lei ^a   Jiang, Hong ^a,c   Tang, Beisha ^a,b,c  

^a CENTRAL SOUTH UNIVERSITY   (China)

^b National Laboratory of Medical Genetics of China   (China)

^c CENTRAL SOUTH UNIVERSITY   (China)

Author keywords

Early onset; Familial Alzheimer's disease; Mutation; Presenilin 1

Indexed keywords

PRESENILIN 1; SERINE;

ADULT; ALZHEIMER DISEASE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHINESE; CODON; CONTROLLED STUDY; EXON; FAMILY; FEMALE; GENE DELETION; GENE MUTATION; GENETIC ANALYSIS; HUMAN; MALE; MOLECULAR GENETICS; MYOCLONUS; ONSET AGE; PATHOGENESIS; PRIORITY JOURNAL; SEIZURE;

ADULT; AGE OF ONSET; ALZHEIMER DISEASE; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION; PEDIGREE; PRESENILIN-1;

EID: 70449518439     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2009.10.055     Document Type: Article

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