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Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies - Dohrn - 2017 - Journal of Neurochemistry - Wiley Online Library
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DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System - Sommen - 2016 - Human Mutation - Wiley Online Library
