Yayici Koken, O. 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 Koken, O., Oztoprak, Ü., Topcu, V., Cavdarli, B., Temuçin, Ç. M., Aydıngöz, Ü., ... Dedeoglu, O.(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 Koken, Ozlem 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 Koken, Ozlem 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 Koken, O. 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={Ozlem Yayici Koken 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} }