The role of hereditary spastic paraplegia related genes in multiple sclerosis: A study of disease susceptibility and clinical outcome

Journal of Neurology

Volumn 254, Issue 9, 2007, Pages 1221-1226

  DeLuca, G C ^a,b   Ramagopalan, S V ^a,b   Cader, M Z ^a,b   Dyment, D A ^a,b   Herrera, B M ^a,b   Orton, S ^a,b   Degenhardt, A ^a   Pugliatti, M ^d   Sadovnick, A D ^c   Sotgiu, S ^d   Ebers, G C ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b UNIVERSITY OF OXFORD   (United Kingdom)

^c UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^d UNIVERSITY OF SASSARI   (Italy)

Author keywords

Genetics; Multiple sclerosis

Indexed keywords

AGED; ARTICLE; ATLASTIN GENE; BSCL2 GENE; COHORT ANALYSIS; CONTROLLED STUDY; DISEASE PREDISPOSITION; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HSPD1 GENE; HUMAN; KIF5A GENE; L1CAM GENE; MAJOR CLINICAL STUDY; MALE; MARKER GENE; MASPARDIN GENE; MULTIPLE SCLEROSIS; NIPA1 GENE; PARAPLEGIN GENE; PLP1 GENE; PRIORITY JOURNAL; SPARTIN GENE; SPASTIN GENE; TREATMENT OUTCOME;

ADENOSINE TRIPHOSPHATASES; ADULT; COHORT STUDIES; DISABILITY EVALUATION; DISEASE PROGRESSION; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HUMANS; MALE; MULTIPLE SCLEROSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; PROGNOSIS; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 36148947887     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-006-0505-4     Document Type: Article

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