Saygi, C. And Sezerman, U. 2019. Seizures, developmental delay, mild intellectual disability, muscular hypotonia, and optic atrophy: About the genetic diagnosis of patient with a novel ATP1A3 mutation. 52nd Conference of the European-Society-of-Human-Genetics (ESHG) , (Gothenburg, Sweden), 1863.

Saygi, C., & Sezerman, U., (2019). Seizures, developmental delay, mild intellectual disability, muscular hypotonia, and optic atrophy: About the genetic diagnosis of patient with a novel ATP1A3 mutation . 52nd Conference of the European-Society-of-Human-Genetics (ESHG) (pp.1863). Gothenburg, Sweden

Saygi, C., And Osman Uğur SEZERMAN. "Seizures, developmental delay, mild intellectual disability, muscular hypotonia, and optic atrophy: About the genetic diagnosis of patient with a novel ATP1A3 mutation," 52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg, Sweden, 2019

Saygi, C. And Sezerman, Osman U. . "Seizures, developmental delay, mild intellectual disability, muscular hypotonia, and optic atrophy: About the genetic diagnosis of patient with a novel ATP1A3 mutation." 52nd Conference of the European-Society-of-Human-Genetics (ESHG) , Gothenburg, Sweden, pp.1863, 2019

Saygi, C. And Sezerman, U. (2019) . "Seizures, developmental delay, mild intellectual disability, muscular hypotonia, and optic atrophy: About the genetic diagnosis of patient with a novel ATP1A3 mutation." 52nd Conference of the European-Society-of-Human-Genetics (ESHG) , Gothenburg, Sweden, p.1863.

@conferencepaper{conferencepaper, author={C. Saygi And author={Osman Uğur SEZERMAN}, title={Seizures, developmental delay, mild intellectual disability, muscular hypotonia, and optic atrophy: About the genetic diagnosis of patient with a novel ATP1A3 mutation}, congress name={52nd Conference of the European-Society-of-Human-Genetics (ESHG)}, city={Gothenburg}, country={Sweden}, year={2019}, pages={1863} }