Erratum: 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
Crossref DOI link: https://doi.org/10.1038/gim.2015.174
Published Print: 2016-01
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Text and Data Mining valid from 2016-01-01
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Article History
First Online: 12 January 2016