A presenilin 1 R278I mutation presenting with language impairment

Neurology

Volumn 63, Issue 9, 2004, Pages 1702-1704

  Godbolt, A K ^a   Beck, J A ^b   Collinge, J ^b   Garrard, P ^c   Warren, J D ^a   Fox, N C ^a   Rossor, M N ^a,d  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

^d NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

PRESENILIN 1;

ADULT; ALZHEIMER DISEASE; ARTICLE; CASE REPORT; CLINICAL FEATURE; DEMENTIA; DISEASE ASSOCIATION; DYSPRAXIA; FAMILIAL DISEASE; FEMALE; GENE MUTATION; GENETIC SCREENING; HUMAN; HUMAN CELL; LANGUAGE DISABILITY; MALE; MEMORY; NEUROPSYCHOLOGY; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; PRIMARY PROGRESSIVE APHASIA; PRIORITY JOURNAL;

EID: 8644276394     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000143060.98164.1A     Document Type: Article

References (10)

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