Yayici Köken, Ö. Et Al. 2021. Expanding the genotype-phenotype spectrum of autosomal recessive charcot-marie-tooth disease: A novel plekhg5 gene mutation. Neurology Asia , vol.26, no.3 , 607-612.

Yayici Köken, Ö., Öztoprak, Ü., Topçu, V., Çavdarli, B., Temuçin, Ç. M., Aydıngöz, Ü., ... Dedeoğlu, Ö.(2021). Expanding the genotype-phenotype spectrum of autosomal recessive charcot-marie-tooth disease: A novel plekhg5 gene mutation. Neurology Asia , vol.26, no.3, 607-612.

Yayici Köken, ÖZLEM Et Al. "Expanding the genotype-phenotype spectrum of autosomal recessive charcot-marie-tooth disease: A novel plekhg5 gene mutation," Neurology Asia , vol.26, no.3, 607-612, 2021

Yayici Köken, ÖZLEM Y. Et Al. "Expanding the genotype-phenotype spectrum of autosomal recessive charcot-marie-tooth disease: A novel plekhg5 gene mutation." Neurology Asia , vol.26, no.3, pp.607-612, 2021

Yayici Köken, Ö. Et Al. (2021) . "Expanding the genotype-phenotype spectrum of autosomal recessive charcot-marie-tooth disease: A novel plekhg5 gene mutation." Neurology Asia , vol.26, no.3, pp.607-612.

@article{article, author={ÖZLEM YAYICI KÖKEN Et Al. }, title={Expanding the genotype-phenotype spectrum of autosomal recessive charcot-marie-tooth disease: A novel plekhg5 gene mutation}, journal={Neurology Asia}, year=2021, pages={607-612} }