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A novel frameshift mutation of C19ORF12 causes NBIA4 with cerebellar atrophy and manifests with severe peripheral motor axonal neuropathy

✍ Scribed by Schottmann, G.; Stenzel, W.; Lützkendorf, S.; Schuelke, M.; Knierim, E.


Book ID
121824124
Publisher
John Wiley and Sons
Year
2013
Tongue
English
Weight
768 KB
Volume
85
Category
Article
ISSN
0009-9163

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