Nauryzbayeva A 1

1. Correction to: Whole-Genome Sequencing Among Kazakhstani Children with Early-Onset Epilepsy Revealed New Gene Variants and Phenotypic Variability (Molecular Neurobiology, (2023), 60, 8, (4324-4335), 10.1007/s12035-023-03346-3)
2. Delayed Diagnosis of Perrault Syndrome: A Rare Genetic Disorder
3. Whole-Genome Sequencing Among Kazakhstani Children with Early-Onset Epilepsy Revealed New Gene Variants and Phenotypic Variability
4. Exploring National Identity Through Modern Monumental and Decorative Tapestry of Kazakhstan
5. Genomic Investigation of Infantile and Childhood Epileptic Encephalopathies in Kazakhstan: An Urgent Priority
6. Elucidating the genomic basis of rare pediatric neurological diseases in Central Asia and Transcaucasia
7. Assessment of Safe Access to Pedestrian Infrastructure Facilities in the City of Almaty, Kazakhstan
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