Genotype-phenotype analysis in early-onset Alzheimer's disease due to presenilin-1 mutations at codon 139

European Journal of Medical Research

Volumn 9, Issue 7, 2004, Pages 361-364

  Hanisch, Frank ^a   Kolmel H W ^b  

^a MARTIN LUTHER UNIVERSITY HALLE WITTENBERG   (Germany)

^b HELIOS KLINIKUM ERFURT   (Germany)

Author keywords

Autosomal dominant early onset Alzheimer's disease; Myoclonia; Presenilin 1

Indexed keywords

MEMBRANE PROTEIN; PRESENILIN 1; PSEN1 PROTEIN, HUMAN;

ADULT; ALZHEIMER DISEASE; ARTICLE; CASE REPORT; CODON; FEMALE; GENETICS; GENOTYPE; HUMAN; MALE; METABOLISM; MIDDLE AGED; MUTATION; PATHOPHYSIOLOGY; PEDIGREE; PHENOTYPE;

ADULT; ALZHEIMER DISEASE; CODON; FEMALE; GENOTYPE; HUMANS; MALE; MEMBRANE PROTEINS; MIDDLE AGED; MUTATION; PEDIGREE; PHENOTYPE; PRESENILIN-1;

EID: 16644386350     PISSN: 09492321     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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