YEŞİL, G. Et Al. 2018. Expanding the Phenotype of Homozygous KCNMA1 Mutations; Dyskinesia, Epilepsy, Intellectual Disability, Cerebellar and Corticospinal Tract Atrophy. BALKAN MEDICAL JOURNAL , vol.35, no.4 , 336-339.

YEŞİL, G., ARALAŞMAK, A., Akyuz, E., Icagasioglu, D., Sahin, T. U., & Bayram, Y., (2018). Expanding the Phenotype of Homozygous KCNMA1 Mutations; Dyskinesia, Epilepsy, Intellectual Disability, Cerebellar and Corticospinal Tract Atrophy. BALKAN MEDICAL JOURNAL , vol.35, no.4, 336-339.

YEŞİL, Gözde Et Al. "Expanding the Phenotype of Homozygous KCNMA1 Mutations; Dyskinesia, Epilepsy, Intellectual Disability, Cerebellar and Corticospinal Tract Atrophy," BALKAN MEDICAL JOURNAL , vol.35, no.4, 336-339, 2018

YEŞİL, Gözde Et Al. "Expanding the Phenotype of Homozygous KCNMA1 Mutations; Dyskinesia, Epilepsy, Intellectual Disability, Cerebellar and Corticospinal Tract Atrophy." BALKAN MEDICAL JOURNAL , vol.35, no.4, pp.336-339, 2018

YEŞİL, G. Et Al. (2018) . "Expanding the Phenotype of Homozygous KCNMA1 Mutations; Dyskinesia, Epilepsy, Intellectual Disability, Cerebellar and Corticospinal Tract Atrophy." BALKAN MEDICAL JOURNAL , vol.35, no.4, pp.336-339.

@article{article, author={Gözde YEŞİL Et Al. }, title={Expanding the Phenotype of Homozygous KCNMA1 Mutations; Dyskinesia, Epilepsy, Intellectual Disability, Cerebellar and Corticospinal Tract Atrophy}, journal={BALKAN MEDICAL JOURNAL}, year=2018, pages={336-339} }