6 results on '"Erdin, Serkan"'
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2. Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models
3. Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models
4. Dystonia-specific mutations in THAP1 alter transcription of genes associated with neurodevelopment and myelin
5. Recurrent De Novo and Biallelic Variation of ATAD3A , Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes
6. Transcriptional Consequences of 16p11.2 Deletion and Duplication in Mouse Cortex and Multiplex Autism Families
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