Çöllü, M. Et Al. 2019. Carnitine palmitoyltransferase II (CPT-II) deficiency: Phenotypic implications of the common mutation S113l.. Society for the Study of Inborn Errors of Metabolism (SSIEM) Annual Symposium , (Rotterdam, Netherlands), 195.

Çöllü, M., Güneş, S., Güneş, D., Balcı, M. C., Demirkol, M., & Gökçay, G. F., (2019). Carnitine palmitoyltransferase II (CPT-II) deficiency: Phenotypic implications of the common mutation S113l. . Society for the Study of Inborn Errors of Metabolism (SSIEM) Annual Symposium (pp.195). Rotterdam, Netherlands

Çöllü, Medis Et Al. "Carnitine palmitoyltransferase II (CPT-II) deficiency: Phenotypic implications of the common mutation S113l.," Society for the Study of Inborn Errors of Metabolism (SSIEM) Annual Symposium, Rotterdam, Netherlands, 2019

Çöllü, Medis Et Al. "Carnitine palmitoyltransferase II (CPT-II) deficiency: Phenotypic implications of the common mutation S113l.." Society for the Study of Inborn Errors of Metabolism (SSIEM) Annual Symposium , Rotterdam, Netherlands, pp.195, 2019

Çöllü, M. Et Al. (2019) . "Carnitine palmitoyltransferase II (CPT-II) deficiency: Phenotypic implications of the common mutation S113l.." Society for the Study of Inborn Errors of Metabolism (SSIEM) Annual Symposium , Rotterdam, Netherlands, p.195.

@conferencepaper{conferencepaper, author={Medis Çöllü Et Al. }, title={Carnitine palmitoyltransferase II (CPT-II) deficiency: Phenotypic implications of the common mutation S113l.}, congress name={ Society for the Study of Inborn Errors of Metabolism (SSIEM) Annual Symposium}, city={Rotterdam}, country={Netherlands}, year={2019}, pages={195} }