Spinocerebellar ataxia 3 and Machado-Joseph disease: Clinical, molecular, and neuropathological features

Annals of Neurology

Volumn 39, Issue 4, 1996, Pages 490-499

  Dürr, Alexandra ^a,e   Stevanin, Giovanni ^a   Cancel, Géraldine ^a   Duyckaerts, Charles ^b   Abbas, Nacer ^a   Didierjean, Olivier ^a   Chneiweiss, Hervé ^a   Benomar, Ali ^d   Lyon Caen, Olivier ^a   Julien, Jean ^c   Serdaru, Michel ^a   Penet, Christiane ^a   Agid, Yves ^a   Brice, Alexis ^a  

^a INSERM   (France)

^b Service de Neuropathologie   (France)

^c Service de Neurologie   (France)

^d IBN SINA HOSPITAL   (Morocco)

^e PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

NUCLEOTIDE;

ADOLESCENT; ADULT; AGED; ALLELE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CEREBELLAR ATAXIA; CLINICAL FEATURE; CONTROLLED STUDY; DYSPHAGIA; FEMALE; GENE MUTATION; HUMAN; MACHADO JOSEPH DISEASE; MAJOR CLINICAL STUDY; MALE; MUSCLE ATROPHY; NEUROPATHOLOGY; NUCLEOTIDE SEQUENCE; ONSET AGE; OPHTHALMOPLEGIA; PRIORITY JOURNAL; TENDON REFLEX;

ADULT; AGE OF ONSET; CENTRAL NERVOUS SYSTEM; FEMALE; GENE FREQUENCY; HUMANS; MACHADO-JOSEPH DISEASE; MALE; MIDDLE AGED; MUTATION; REPETITIVE SEQUENCES, NUCLEIC ACID; SPINOCEREBELLAR DEGENERATIONS;

EID: 9244225693     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410390411     Document Type: Article

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