Kocoglu, C. Et Al. 2018. Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families. NEUROLOGY-GENETICS , vol.4, no.1 .

Kocoglu, C., Gundogdu, A., Kocaman, G., KAHRAMAN KOYTAK, P., ULUÇ, K., Kiziltan, G., ... ÇAĞLAYAN, A. O.(2018). Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families. NEUROLOGY-GENETICS , vol.4, no.1.

Kocoglu, Cemile Et Al. "Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families," NEUROLOGY-GENETICS , vol.4, no.1, 2018

Kocoglu, Cemile Et Al. "Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families." NEUROLOGY-GENETICS , vol.4, no.1, 2018

Kocoglu, C. Et Al. (2018) . "Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families." NEUROLOGY-GENETICS , vol.4, no.1.

@article{article, author={Cemile Kocoglu Et Al. }, title={Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families}, journal={NEUROLOGY-GENETICS}, year=2018}