Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disability
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| Description | scientific article published in December 2014 |
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author: Brett Copeland Stacey Gabriel Joseph G Gleeson Maha Zaki |
| Publication date | December 1, 2014 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |