A novel FBXO28 frameshift mutation in a child with developmental delay, dysmorphic features, and intractable epilepsy: A second gene that may contribute to the 1q41-q42 deletion phenotype
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| Description | scientific article published on 01 July 2018 |
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author: Isabelle Schrauwen Ignazio Stefano Piras Chris Balak S Rangasamy |
| Publication date | July 1, 2018 |
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