Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies.
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| Description | scientific article |
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author: Jörg B. Schulz Maike F Dohrn Kristl G Claeys Istvan Katona Stefan Wolking |
| Publication date | November 7, 2017 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |