Statistics for Genetic mosaicism, intrafamilial phenotypic heterogeneity, and molecular defects of a novel missense SLC6A1 mutation associated with epilepsy and ADHD
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| java.util.UUID:a94a7d9d-df77-4712-ad2f-50f7caf6c530 | 20 |
| java.util.UUID:8c4d4ebe-355d-47e1-8522-46a3325d0cec | 16 |
| Poliquin2021Genetic-AAM.pdf | 7 |
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