Ozlem Capan-Yalcın
Tekirdag, Turkey
Last Updated: 09/26/2026
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Found 8 publications
Comprehensive in Silico Reclassification of MECP2 Variants of Uncertain Significance in Rett Syndrome: Performance Evaluation and Structural Analysis.
Journal: Journal of molecular neuroscience : MN
Published: June 20, 2025
Navigating Uncertainty: Assessing Variants of Uncertain Significance in the CDKL5 Gene for Developmental and Epileptic Encephalopathy Using In Silico Prediction Tools and Computational Analysis.
Journal: Journal of molecular neuroscience : MN
Published: October 12, 2024
A Review of Functional Characterization of Single Amino Acid Change Mutations in HNF Transcription Factors in MODY Pathogenesis.
Journal: The protein journal
Published: April 22, 2021
HNF1A-MODY Mutations in Nuclear Localization Signal Impair HNF1A-Import Receptor KPNA6 Interactions.
HNF1A-MODY Mutations in Nuclear Localization Signal Impair HNF1A-Import Receptor KPNA6 Interactions.
Journal: The protein journal
Published: December 28, 2020
Whole exome sequencing reveals novel candidate gene variants for MODY.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: May 28, 2020
SCN1A gene sequencing in 46 Turkish epilepsy patients disclosed 12 novel mutations.
Journal: Seizure
Published: January 26, 2016
Showing 1-8 of 8
Last Updated: 09/26/2026