GPT2 mutations cause developmental encephalopathy with microcephaly and features of complicated hereditary spastic paraplegia
Author:
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Hengel, H.; Keimer, R.; Deigendesch, W.; Riess, A.; Marzouqa, H.; Zaidan, J.; Bauer, P.; Schoels, L.
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Tübinger Autor(en):
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Published in:
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Clinical Genetics
(2018), Bd.
94,
H.
3-4,
S.
356-361
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Verlagsangabe:
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Wiley
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Language:
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English
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Full text:
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http://dx.doi.org/10.1111/cge.13390
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ISSN:
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1399-0004
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DDC Classifikation:
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570 - Life sciences; biology 610 - Medicine and health
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Dokumentart:
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Article
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Show full item record
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