Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability
- 1 December 2014
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 95 (6), 721-728
- https://doi.org/10.1016/j.ajhg.2014.10.016
Abstract
No abstract availableThis publication has 31 references indexed in Scilit:
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