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

DSpace Repository

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: Artikel
Show full item record

This item appears in the following Collection(s)