GPT2 mutations cause developmental encephalopathy with microcephaly and features of complicated hereditary spastic paraplegia

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GPT2 mutations cause developmental encephalopathy with microcephaly and features of complicated hereditary spastic paraplegia

Author: Hengel, H.; Keimer, R.; Deigendesch, W.; Riess, A.; Marzouqa, H.; Zaidan, J.; Bauer, P.; Schoels, L.
Tübinger Autor(en):
Hengel, Holger
Riess, Angelika
Bauer, Peter
Schöls, Ludger
Published in: Clinical Genetics (2018), Bd. 94, H. 3-4, S. 356-361
Verlagsangabe: Wiley
Language: English
Full text: http://dx.doi.org/10.1111/cge.13390
ISSN: 1399-0004
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Article
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