DOI:
10.1055/s-00000032
Klinische Neurophysiologie
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References
Dohrn MF, Glockle N, Mulahasanovic L. et al.
Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies.
J Neurochem 2017;
143: 507-522
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