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Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability
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| Zeitschriftentitel: | Neurology Genetics |
|---|---|
| Personen und Körperschaften: | , , , , , , , |
| In: | Neurology Genetics, 2, 2016, 5 |
| Format: | E-Article |
| Sprache: | Englisch |
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Ovid Technologies (Wolters Kluwer Health)
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Steinrücke, Sofia Lohmann, Katja Domingo, Aloysius Rolfs, Arndt Bäumer, Tobias Spiegler, Juliane Hartmann, Corinna Münchau, Alexander Steinrücke, Sofia Lohmann, Katja Domingo, Aloysius Rolfs, Arndt Bäumer, Tobias Spiegler, Juliane Hartmann, Corinna Münchau, Alexander |
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Steinrücke, Sofia Lohmann, Katja Domingo, Aloysius Rolfs, Arndt Bäumer, Tobias Spiegler, Juliane Hartmann, Corinna Münchau, Alexander |
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Steinrücke, Sofia Lohmann, Katja Domingo, Aloysius Rolfs, Arndt Bäumer, Tobias Spiegler, Juliane Hartmann, Corinna Münchau, Alexander Neurology Genetics Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability Genetics (clinical) Neurology (clinical) |
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steinrücke, sofia |
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Steinrücke, Sofia Lohmann, Katja Domingo, Aloysius Rolfs, Arndt Bäumer, Tobias Spiegler, Juliane Hartmann, Corinna Münchau, Alexander 2376-7839 Ovid Technologies (Wolters Kluwer Health) Genetics (clinical) Neurology (clinical) http://dx.doi.org/10.1212/nxg.0000000000000106 Novel <i>GNB1</i> missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability Neurology Genetics |
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| title |
Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability |
| title_unstemmed |
Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability |
| title_full |
Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability |
| title_fullStr |
Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability |
| title_full_unstemmed |
Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability |
| title_short |
Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability |
| title_sort |
novel
<i>gnb1</i>
missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability |
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Genetics (clinical) Neurology (clinical) |
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| spelling | Steinrücke, Sofia Lohmann, Katja Domingo, Aloysius Rolfs, Arndt Bäumer, Tobias Spiegler, Juliane Hartmann, Corinna Münchau, Alexander 2376-7839 Ovid Technologies (Wolters Kluwer Health) Genetics (clinical) Neurology (clinical) http://dx.doi.org/10.1212/nxg.0000000000000106 Novel <i>GNB1</i> missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability Neurology Genetics |
| spellingShingle | Steinrücke, Sofia, Lohmann, Katja, Domingo, Aloysius, Rolfs, Arndt, Bäumer, Tobias, Spiegler, Juliane, Hartmann, Corinna, Münchau, Alexander, Neurology Genetics, Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability, Genetics (clinical), Neurology (clinical) |
| title | Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability |
| title_full | Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability |
| title_fullStr | Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability |
| title_full_unstemmed | Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability |
| title_short | Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability |
| title_sort | novel <i>gnb1</i> missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability |
| title_unstemmed | Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability |
| topic | Genetics (clinical), Neurology (clinical) |
| url | http://dx.doi.org/10.1212/nxg.0000000000000106 |