Acar, F. A. Et Al. 2019. Antenatal Bartter Syndrome Caused by a Novel Homozygous Mutation in SLC12A1 Gene. INDIAN JOURNAL OF NEPHROLOGY , vol.29, no.5 , 360-363.

Acar, F. A., Isik, G., MUTLU, M., KADER, Ş., ASLAN, Y., & KALYONCU, M., (2019). Antenatal Bartter Syndrome Caused by a Novel Homozygous Mutation in SLC12A1 Gene. INDIAN JOURNAL OF NEPHROLOGY , vol.29, no.5, 360-363.

Acar, Filiz Et Al. "Antenatal Bartter Syndrome Caused by a Novel Homozygous Mutation in SLC12A1 Gene," INDIAN JOURNAL OF NEPHROLOGY , vol.29, no.5, 360-363, 2019

Acar, Filiz A. Et Al. "Antenatal Bartter Syndrome Caused by a Novel Homozygous Mutation in SLC12A1 Gene." INDIAN JOURNAL OF NEPHROLOGY , vol.29, no.5, pp.360-363, 2019

Acar, F. A. Et Al. (2019) . "Antenatal Bartter Syndrome Caused by a Novel Homozygous Mutation in SLC12A1 Gene." INDIAN JOURNAL OF NEPHROLOGY , vol.29, no.5, pp.360-363.

@article{article, author={Filiz Akturk Acar Et Al. }, title={Antenatal Bartter Syndrome Caused by a Novel Homozygous Mutation in SLC12A1 Gene}, journal={INDIAN JOURNAL OF NEPHROLOGY}, year=2019, pages={360-363} }