H. Mutlu-Albayrak Et Al. , "Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect.," Case reports in genetics , vol.2015, pp.259627, 2015
Mutlu-Albayrak, H. Et Al. 2015. Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect.. Case reports in genetics , vol.2015 , 259627.
Mutlu-Albayrak, H., Bene, J., Oflaz, M. B., Tanyalçın, T., Çaksen, H., & Melegh, B., (2015). Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect.. Case reports in genetics , vol.2015, 259627.
Mutlu-Albayrak, HATİCE Et Al. "Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect.," Case reports in genetics , vol.2015, 259627, 2015
Mutlu-Albayrak, HATİCE Et Al. "Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect.." Case reports in genetics , vol.2015, pp.259627, 2015
Mutlu-Albayrak, H. Et Al. (2015) . "Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect.." Case reports in genetics , vol.2015, p.259627.
@article{article, author={HATİCE MUTLU Et Al. }, title={Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect.}, journal={Case reports in genetics}, year=2015, pages={259627} }