D. YÜCEL YILMAZ Et Al. , "OCTN2 Gene Mutations in Turkish Patients with Primary Carnitine Deficiency," 2012 Annual Symposium of the Society for the Study of Inborn Errors of Metabolism-United Kingdom , 2012
YÜCEL YILMAZ, D. Et Al. 2012. OCTN2 Gene Mutations in Turkish Patients with Primary Carnitine Deficiency. 2012 Annual Symposium of the Society for the Study of Inborn Errors of Metabolism-United Kingdom .
YÜCEL YILMAZ, D., ERSOY, M., CANDAN, Ş., BALCI, M. C., KILIÇ, M., GÖKÇAY, G., ... DURSUN, A.(2012). OCTN2 Gene Mutations in Turkish Patients with Primary Carnitine Deficiency . 2012 Annual Symposium of the Society for the Study of Inborn Errors of Metabolism-United Kingdom
YÜCEL YILMAZ, DİDEM Et Al. "OCTN2 Gene Mutations in Turkish Patients with Primary Carnitine Deficiency," 2012 Annual Symposium of the Society for the Study of Inborn Errors of Metabolism-United Kingdom, 2012
YÜCEL YILMAZ, DİDEM Y. Et Al. "OCTN2 Gene Mutations in Turkish Patients with Primary Carnitine Deficiency." 2012 Annual Symposium of the Society for the Study of Inborn Errors of Metabolism-United Kingdom , 2012
YÜCEL YILMAZ, D. Et Al. (2012) . "OCTN2 Gene Mutations in Turkish Patients with Primary Carnitine Deficiency." 2012 Annual Symposium of the Society for the Study of Inborn Errors of Metabolism-United Kingdom .
@conferencepaper{conferencepaper, author={DİDEM YÜCEL YILMAZ Et Al. }, title={OCTN2 Gene Mutations in Turkish Patients with Primary Carnitine Deficiency}, congress name={2012 Annual Symposium of the Society for the Study of Inborn Errors of Metabolism-United Kingdom}, city={}, country={}, year={2012}}