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Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6.

par Globas, C;du Montcel, S Tezenas;Balikó, Lazlo;Boesch, S;Depondt, Chantal ;Didonato, Stefano;Dürr, Alexandra;Filla, A;Klockgether, T;Mariotti, Christian;Melegh, Bela;Rakowicz, M;Ribaï, Pascale;Rola, R;Schmitz-Hübsch, T;Szymanski, S;Timmann, D;van de Warrenburg, B P;Bauer, Peter;Schöls, Lüdger
Référence Movement disorders, 23, 15, page (2232-2238)
Publication Publié, 2008-11

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Titre:	Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6.
Auteur:	Globas, C; du Montcel, S Tezenas; Balikó, Lazlo; Boesch, S; Depondt, Chantal; Didonato, Stefano; Dürr, Alexandra; Filla, A; Klockgether, T; Mariotti, Christian; Melegh, Bela; Rakowicz, M; Ribaï, Pascale; Rola, R; Schmitz-Hübsch, T; Szymanski, S; Timmann, D; van de Warrenburg, B P; Bauer, Peter; Schöls, Lüdger
Informations sur la publication:	Movement disorders, 23, 15, page (2232-2238)
Statut de publication:	Publié, 2008-11
Sujet CREF:	Neurologie
Mots-clés:	CAG repeat expansion
	Determinants of age at onset
	Early symptoms
	Spinocerebellar ataxia
MeSH keywords:	Adolescent
	Adult
	Aged
	Aged, 80 and over
	Calcium Channels -- genetics
	DNA Mutational Analysis
	Female
	Gait Disorders, Neurologic -- complications
	Humans
	Linear Models
	Male
	Middle Aged
	Nerve Tissue Proteins -- genetics
	Nuclear Proteins -- genetics
	Repressor Proteins -- genetics
	Spinocerebellar Ataxias -- classification -- complications -- genetics
	Trinucleotide Repeat Expansion -- genetics
	Young Adult
Note générale:	Journal Article
	Research Support, Non-U.S. Gov't
	FLWIN
Langue:	Anglais
Identificateurs:	urn:issn:0885-3185
	info:doi/10.1002/mds.22288
	info:scp/61449101789
	info:pmid/18759344