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
Genet Med
.
2016 Jan;18(1):108.
doi: 10.1038/gim.2015.174.
PMID:
26754338
DOI:
10.1038/gim.2015.174
No abstract available
Publication types
Published Erratum