Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation

Neurology

Volumn 55, Issue 1, 2000, Pages 89-94

  White, K D ^a   Ince, P G ^b   Lusher, M ^a   Lindsey, J ^a   Cookson, M ^b   Bashir, R ^a   Shaw, P J ^a   Bushby, K M D ^a,c  

^a NEWCASTLE UNIVERSITY   (United Kingdom)

^b NEWCASTLE GENERAL HOSPITAL   (United Kingdom)

^c Department of Human Genetics ^*  (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; DNA; MUTANT PROTEIN; SPASTIN; UNCLASSIFIED DRUG;

ADULT; AGED; ARTICLE; AUTOPSY; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 2P; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DEMENTIA; DISEASE CLASSIFICATION; FEMALE; HAPLOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN TISSUE; LEARNING DISORDER; LEWY BODY; MALE; NEUROFIBRILLARY TANGLE; ONSET AGE; PRIORITY JOURNAL; UNITED KINGDOM;

EID: 0034641262     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.55.1.89     Document Type: Article

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