Dilan Genç-Akdağ

2PUBLICATIONS
9CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Neurogenetics
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Publications (2)

|Oct 08, 2026
Genotype-phenotype variability in TRMT10A deficiency: divergent developmental outcomes associated with biallelic loss-of-function variants.

|Feb 18, 2026
Keipert syndrome beyond classical features: novel GPC4 variant associated with epilepsy but preserved cognition.

Hilmi Bolat, Hilal Aydın, Dilan Genç-Akdağ

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Hilmi Bolat

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Hilal Aydın

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Hamide Betül Gerik-Çelebi

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Gül Ünsel-Bolat