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Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disability
scientific article published in December 2014
Author/s
author: Maha Zaki, Brett Copeland, Stacey Gabriel, Joseph G Gleeson
Work details
Publication date
December 1, 2014
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Language
English
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