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FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia.

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Title: FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia.
Authors: Brussino A; Dipartimento di Genetica, Biologia e Biochimica, Università degli Studi di Torinoand S.C. Genetica Medica, Ospedale San Giovanni Battista di Torino, Turin, Italy. alfredo.brusco@unito.it, Gellera C, Saluto A, Mariotti C, Arduino C, Castellotti B, Camerlingo M, de Angelis V, Orsi L, Tosca P, Migone N, Taroni F, Brusco A
Source: Neurology [Neurology] 2005 Jan 11; Vol. 64 (1), pp. 145-7.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0401060 Publication Model: Print Cited Medium: Internet ISSN: 1526-632X (Electronic) Linking ISSN: 00283878 NLM ISO Abbreviation: Neurology Subsets: MEDLINE
Database: MEDLINE Ultimate
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PubType: Academic Journal
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  Data: FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia.
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  Data: <searchLink fieldCode="AU" term="%22Brussino+A%22">Brussino A</searchLink>; Dipartimento di Genetica, Biologia e Biochimica, Università degli Studi di Torinoand S.C. Genetica Medica, Ospedale San Giovanni Battista di Torino, Turin, Italy. alfredo.brusco@unito.it<br /><searchLink fieldCode="AU" term="%22Gellera+C%22">Gellera C</searchLink><br /><searchLink fieldCode="AU" term="%22Saluto+A%22">Saluto A</searchLink><br /><searchLink fieldCode="AU" term="%22Mariotti+C%22">Mariotti C</searchLink><br /><searchLink fieldCode="AU" term="%22Arduino+C%22">Arduino C</searchLink><br /><searchLink fieldCode="AU" term="%22Castellotti+B%22">Castellotti B</searchLink><br /><searchLink fieldCode="AU" term="%22Camerlingo+M%22">Camerlingo M</searchLink><br /><searchLink fieldCode="AU" term="%22de+Angelis+V%22">de Angelis V</searchLink><br /><searchLink fieldCode="AU" term="%22Orsi+L%22">Orsi L</searchLink><br /><searchLink fieldCode="AU" term="%22Tosca+P%22">Tosca P</searchLink><br /><searchLink fieldCode="AU" term="%22Migone+N%22">Migone N</searchLink><br /><searchLink fieldCode="AU" term="%22Taroni+F%22">Taroni F</searchLink><br /><searchLink fieldCode="AU" term="%22Brusco+A%22">Brusco A</searchLink>
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  Data: <searchLink fieldCode="JN" term="%220401060%22">Neurology</searchLink> [Neurology] 2005 Jan 11; Vol. 64 (1), pp. 145-7.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Lippincott+Williams+%26+Wilkins%22">Lippincott Williams & Wilkins </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>0401060 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1526-632X (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200283878%22">00283878 </searchLink><i>NLM ISO Abbreviation: </i>Neurology <i>Subsets: </i>MEDLINE
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        Value: 10.1212/01.WNL.0000148723.37489.3F
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      – Code: eng
        Text: English
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      – TitleFull: FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia.
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              Text: 2005 Jan 11
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