Hereditary myoclonus dystonia (DYT11): A novel SGCE gene mutation with intrafamilial phenotypic heterogeneity
Identifieur interne : 002150 ( Istex/Curation ); précédent : 002149; suivant : 002151Hereditary myoclonus dystonia (DYT11): A novel SGCE gene mutation with intrafamilial phenotypic heterogeneity
Auteurs : Sui H. Wong [Royaume-Uni] ; Malcolm J. Steiger [Royaume-Uni] ; Andrew J. Larner [Royaume-Uni] ; Nicholas A. Fletcher [Royaume-Uni]Source :
- Movement Disorders [ 0885-3185 ] ; 2010-05-15.
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DOI: 10.1002/mds.23037
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Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="2010-05-15">2010-05-15</date><biblScope unit="vol">25</biblScope><biblScope unit="issue">7</biblScope><biblScope unit="page" from="956">956</biblScope><biblScope unit="page" to="957">957</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">05043D5EA6E1C38AF9D4C03E0B7E9E2DB9574EF9</idno><idno type="DOI">10.1002/mds.23037</idno><idno type="ArticleID">MDS23037</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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