Targeted High-Throughput Sequencing Identifies Mutations in atlastin-1 as a Cause of Hereditary Sensory Neuropathy Type I
Open Access
- 7 January 2011
- journal article
- research article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 88 (1), 99-105
- https://doi.org/10.1016/j.ajhg.2010.12.003
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
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