Statistics for De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder
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| De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder | 201 |
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| java.util.UUID:a7ec6385-35f6-4f53-a18f-a89b9a699630 | 28 |
| java.util.UUID:ebc2f2db-cfc1-48e3-b118-2e332128aeea | 19 |
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