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):

Published in:

Clinical Genetics (2018), Bd. 94, H. 3-4, S. 356-361

Verlagsangabe:

Wiley

Language:

English

Full text:

ISSN:

1399-0004

DDC Classifikation:

570 - Life sciences; biology
610 - Medicine and health

Dokumentart:

Article

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