Kaya Bilguvar · researcher · YYNN

Kaya Bilguvar

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researcher

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Works
3

Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy

scientific journal article

A novel de novo mutation in ATP1A3 and childhood-onset schizophrenia

scientific article published on September 2016

Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism

scientific article published on 14 December 2011

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