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M A Knight

Showing results (21-30 of 24) with videos related to

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Neurology|December 13, 2006
Spinocerebellar ataxia type 20 is genetically distinct from spinocerebellar ataxia type 5D N Lorenzo, S M Forrest, Y Ikeda, et al.
Neurology|November 28, 2001
A new autosomal dominant pure cerebellar ataxiaE Storey, R J Gardner, M A Knight, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2005
Spinocerebellar ataxia type 14: study of a family with an exon 5 mutation in the PRKCG geneM C Fahey, M A Knight, J H Shaw, et al.
Neuroreport|April 20, 1999
Early-onset Alzheimer's disease caused by a novel mutation at codon 219 of the presenilin-1 geneM J Smith, R J Gardner, M A Knight, et al.
Pageof 3

Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
Neurology|December 13, 2006
Spinocerebellar ataxia type 20 is genetically distinct from spinocerebellar ataxia type 5D N Lorenzo, S M Forrest, Y Ikeda, et al.
Neurology|November 28, 2001
A new autosomal dominant pure cerebellar ataxiaE Storey, R J Gardner, M A Knight, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2005
Spinocerebellar ataxia type 14: study of a family with an exon 5 mutation in the PRKCG geneM C Fahey, M A Knight, J H Shaw, et al.
Neuroreport|April 20, 1999
Early-onset Alzheimer's disease caused by a novel mutation at codon 219 of the presenilin-1 geneM J Smith, R J Gardner, M A Knight, et al.
Pageof 3