Mammadova, D. 2021. Cortical Blindness and Epileptic Encephalopathy Due to a Previously Unknown Compound Heterozygous DIAPH1 Gene Mutation. Abstracts of the 46th Annual Meeting of the Society for Neuropediatrics , (Stuttgart, Germany), 52.

Mammadova, D., (2021). Cortical Blindness and Epileptic Encephalopathy Due to a Previously Unknown Compound Heterozygous DIAPH1 Gene Mutation . Abstracts of the 46th Annual Meeting of the Society for Neuropediatrics (pp.52). Stuttgart, Germany

Mammadova, Dilfara. "Cortical Blindness and Epileptic Encephalopathy Due to a Previously Unknown Compound Heterozygous DIAPH1 Gene Mutation," Abstracts of the 46th Annual Meeting of the Society for Neuropediatrics, Stuttgart, Germany, 2021

Mammadova, Dilfara. "Cortical Blindness and Epileptic Encephalopathy Due to a Previously Unknown Compound Heterozygous DIAPH1 Gene Mutation." Abstracts of the 46th Annual Meeting of the Society for Neuropediatrics , Stuttgart, Germany, pp.52, 2021

Mammadova, D. (2021) . "Cortical Blindness and Epileptic Encephalopathy Due to a Previously Unknown Compound Heterozygous DIAPH1 Gene Mutation." Abstracts of the 46th Annual Meeting of the Society for Neuropediatrics , Stuttgart, Germany, p.52.

@conferencepaper{conferencepaper, author={Dilfara Məmmədova}, title={Cortical Blindness and Epileptic Encephalopathy Due to a Previously Unknown Compound Heterozygous DIAPH1 Gene Mutation}, congress name={Abstracts of the 46th Annual Meeting of the Society for Neuropediatrics}, city={Stuttgart}, country={Germany}, year={2021}, pages={52} }