A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's disease.

Human mutation

Volumn 16, Issue 1, 2000, Pages 95-

  Raux, G ^a   Gantier, R ^a   Martin, C ^a   Pothin, Y ^a   Brice, A ^a   Frebourg, T ^a   Campion, D ^a  

^a INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

LEUCINE; MEMBRANE PROTEIN; PRESENILIN 1; PSEN1 PROTEIN, HUMAN; VALINE;

ADULT; ALZHEIMER DISEASE; AMINO ACID SUBSTITUTION; ARTICLE; DOMINANT GENE; FEMALE; FRANCE; GENETICS; HUMAN; MALE; MISSENSE MUTATION;

ADULT; ALZHEIMER DISEASE; AMINO ACID SUBSTITUTION; FEMALE; FRANCE; GENES, DOMINANT; HUMANS; LEUCINE; MALE; MEMBRANE PROTEINS; MUTATION, MISSENSE; PRESENILIN-1; VALINE;

EID: 0034223610     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/1098-1004(200007)16:1<95::aid-humu28>3.0.co;2-h     Document Type: Article

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