Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene
Identifieur interne : 002C42 ( Istex/Checkpoint ); précédent : 002C41; suivant : 002C43Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene
Auteurs : Peter P. Pramstaller [Italie] ; Bernhard Kis [Italie, Allemagne] ; Cordula Eskelson [Allemagne] ; Katja Hedrich [Allemagne] ; Monika Scherer [Italie] ; Eberhard Schwinger [Allemagne] ; Xandra O. Breakefield [États-Unis] ; Patricia L. Kramer [États-Unis] ; Laurie J. Ozelius [États-Unis] ; Christine Klein [Allemagne]Source :
- Movement Disorders [ 0885-3185 ] ; 2002-03.
Url:
DOI: 10.1002/mds.10071
Affiliations:
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ISTEX:F9E1F40464C0CBD05E6CF46EC3C35B9835DF1D89Le document en format XML
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