A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia

Rydning, S. L.; Dudesek, A.; Rimmele, F.; Funke, C.; Krueger, S.; Biskup, S.; Vigeland, M. D.; Hjorthaug, H. S.; Sejersted, Y.; Tallaksen, C.; Selmer, K. K.; Kamm, C.

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A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia

Author:

Rydning, S. L.; Dudesek, A.; Rimmele, F.; Funke, C.; Krueger, S.; Biskup, S.; Vigeland, M. D.; Hjorthaug, H. S.; Sejersted, Y.; Tallaksen, C.; Selmer, K. K.; Kamm, C.

Tübinger Autor(en):

Biskup, Saskia

Published in:

European Journal of Neurology (2018), Bd. 25, H. 7, S. 943-

Verlagsangabe:

Wiley

Language:

English

Full text:

http://dx.doi.org/10.1111/ene.13625

ISSN:

1468-1331

DDC Classifikation:

610 - Medicine and health
570 - Life sciences; biology

Dokumentart:

Article

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4 Medizinische Fakultät [31284]
8 Zentrale, interfakultäre und fakultätsübergreifende Einrichtungen [12355]

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A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia

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A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia

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