U. Spiekerkoetter Et Al. , "Silent and symptomatic primary carnitine deficiency within the same family due to identical mutations in the organic cation/carnitine transporter OCTN2.," Journal of inherited metabolic disease , vol.26, no.6, pp.613-5, 2003
Spiekerkoetter, U. Et Al. 2003. Silent and symptomatic primary carnitine deficiency within the same family due to identical mutations in the organic cation/carnitine transporter OCTN2.. Journal of inherited metabolic disease , vol.26, no.6 , 613-5.
Spiekerkoetter, U., Huener, G. F., Baykal, T., Demirkol, M., Duran, M., Wanders, R., ... Nezu, J.(2003). Silent and symptomatic primary carnitine deficiency within the same family due to identical mutations in the organic cation/carnitine transporter OCTN2.. Journal of inherited metabolic disease , vol.26, no.6, 613-5.
Spiekerkoetter, U Et Al. "Silent and symptomatic primary carnitine deficiency within the same family due to identical mutations in the organic cation/carnitine transporter OCTN2.," Journal of inherited metabolic disease , vol.26, no.6, 613-5, 2003
Spiekerkoetter, U Et Al. "Silent and symptomatic primary carnitine deficiency within the same family due to identical mutations in the organic cation/carnitine transporter OCTN2.." Journal of inherited metabolic disease , vol.26, no.6, pp.613-5, 2003
Spiekerkoetter, U. Et Al. (2003) . "Silent and symptomatic primary carnitine deficiency within the same family due to identical mutations in the organic cation/carnitine transporter OCTN2.." Journal of inherited metabolic disease , vol.26, no.6, pp.613-5.
@article{article, author={U Spiekerkoetter Et Al. }, title={Silent and symptomatic primary carnitine deficiency within the same family due to identical mutations in the organic cation/carnitine transporter OCTN2.}, journal={Journal of inherited metabolic disease}, year=2003, pages={613-5} }