Presenilin-1 mutations in alzheimer's disease: An update on genotype-phenotype relationships

Journal of Alzheimer's Disease

Volumn 37, Issue 4, 2013, Pages 653-659

  Larner, A J ^a  

^a WALTON CENTRE FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

Author keywords

Alzheimer's disease; mutation; presenilin 1

Indexed keywords

ALZHEIMER DISEASE; APHASIA; CEREBELLAR ATAXIA; EXON; EXTRAPYRAMIDAL SYMPTOM; FRONTOTEMPORAL DEMENTIA; GENE; GENE DELETION; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; LANGUAGE DISABILITY; PARKINSONISM; PHENOTYPE; PRESENILIN 1 GENE; PRIORITY JOURNAL; PROTEIN FUNCTION; REVIEW; SEIZURE; SPASTIC PARAPLEGIA;

ALZHEIMER'S DISEASE; MUTATION; PRESENILIN 1;

ALZHEIMER DISEASE; ANIMALS; GENOTYPE; HUMANS; PHENOTYPE; PRESENILIN-1;

EID: 84892733664     PISSN: 13872877     EISSN: 18758908     Source Type: Journal    
DOI: 10.3233/JAD-130746     Document Type: Review

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