PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia

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PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia

Author: Ozes, B.; Karagoz, N.; Schuele, R.; Rebelo, A.; Sobrido, M. -J.; Harmuth, F.; Synofzik, M.; Pascual, S. I. P.; Colak, M.; Ciftci-Kavaklioglu, B.; Kara, B.; Ordonez-Ugalde, A.; Quintans, B.; Gonzalez, M. A.; Soysal, A.; Zuchner, S.; Battaloglu, E.
Tübinger Autor(en):
Schüle-Freyer, Rebecca
Harmuth, Florian
Synofzik, Matthis
Published in: Clinical Genetics (2017), Bd. 92, H. 5, S. 534-539
Verlagsangabe: Wiley
Language: English
Full text: http://dx.doi.org/10.1111/cge.13008
ISSN: 1399-0004
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Article
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