GlyT1 encephalopathy: Characterization of presumably disease causing GlyT1 mutations

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GlyT1 encephalopathy: Characterization of presumably disease causing GlyT1 mutations

Author: Hauf, K.; Barsch, L.; Bauer, D.; Buchert, R.; Armbruster, A.; Frauenfeld, L.; Grasshoff, U.; Eulenburg, V
Tübinger Autor(en):
Buchert, Rebecca
Frauenfeld, Leonie
Grasshoff, Ute
Published in: Neurochemistry International (2020), Bd. 139, Article 104813
Verlagsangabe: Pergamon - Elsevier Science Ltd
Language: English
Full text: http://dx.doi.org/10.1016/j.neuint.2020.104813
ISSN: 1872-9754
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Article
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