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G. Schottmann, W. Stenzel, S. Lützkendorf, M. Schuelke and E. Knierim A novel frameshift mutation of C19ORF12 causes NBIA4 with cerebellar atrophy and manifests with severe peripheral motor axonal neuropathy Clinical Genetics 85

Version of Record online: 25 MAR 2013 | DOI: 10.1111/cge.12137

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