Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencing.
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| Description | scientific article published on 22 October 2015 |
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author: Magdalena Zimon Dahlia M Kancheva Derek Atkinson Alejandro Estrada Cuzcano Peter De Rijk |
| Publication date | October 22, 2015 |
| Language | English |
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