Molecular and clinical correlations in spinocerebellar ataxia 2: A study of 32 families

Human Molecular Genetics

Volumn 6, Issue 5, 1997, Pages 709-715

  Cancel, Géraldine ^a   Dürr, Alexandra ^a   Didierjean, Olivier ^a   Imbert, Georges ^b   Bürk, Katrin ^c   Lezin, Agnès ^d   Belal, Samir ^e   Benomar, Ali ^f   Abada Bendib, Myriem ^g   Vial, Christophe ^h   Guimarães, João ⁱ   Chneiweiss, Hervé ^j   Stevanin, Giovanni ^a   Yvert, Gael ^b   Abbas, Nacer ^a   Saudou, Frédéric ^b   Lebre, Anne Sophie ^a   Yahyaoui, Mohamed ^f   Hentati, Fayçal ^e   Vernant, Jean Claude ^d   Klockgether, Thomas ^c   Mandel, Jean Louis ^b   Agid, Yves ^a   Brice, Alexis ^a   more..

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

^c UNIVERSITY OF TÜBINGEN   (Germany)

^d CENTRE HOSPITALIER UNIVERSITAIRE DE FORT DE FRANCE   (France)

^e Institut National de Neurologie Tunisia   (Tunisia)

^f IBN SINA HOSPITAL   (Morocco)

^g Centre Hospitalier et Universitaire de Beni Messous Algiers   (Algeria)

^h HÔPITAL NEUROLOGIQUE   (France)

ⁱ HOSPITAL EGAS MONIZ   (Portugal)

^j l'alimentation et l'Environnement   (France)

more..

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CEREBELLAR ATAXIA; CLINICAL FEATURE; DISEASE DURATION; DYSTONIA; FEMALE; GENE MUTATION; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; MOSAICISM; MYOCLONUS; MYOKYMIA; ONSET AGE; PRIORITY JOURNAL; SPERM; TRINUCLEOTIDE REPEAT;

ATAXIA;

EID: 8244220324     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/6.5.709     Document Type: Article

References (37)

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