Exome sequencing identifies novel missense and deletion variants in RTN4IP1 associated with optic atrophy, global developmental delay, epilepsy, ataxia, and choreoathetosis
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| Description | scientific article published on 09 October 2020 |
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author: Gerard Berry Alissa M D'Gama Wen-Hann Tan Monica H Wojcik |
| Publication date | October 9, 2020 |
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