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HARVARD Citation
Dohrn, M. et al. (2017). Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies. Journal of neurochemistry. 143 (5), pp. 507-522. [Online].
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Dohrn, M. et al. (2017). Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies. Journal of neurochemistry. 143 (5), pp. 507-522. [Online].