HAYTOĞLU, Z. Et Al. 2021. Lipin1deficiency: A novel mutation in a patient with recurrent habdomyolysis. XIV International Congress of Inborn Errors of Metabolism , (Australia).

HAYTOĞLU, Z., KOR, D., BULUT, F. D., KILAVUZ, S., KARA, E., KÖŞECİ, B., ... BURKAÇ, E.(2021). Lipin1deficiency: A novel mutation in a patient with recurrent habdomyolysis . XIV International Congress of Inborn Errors of Metabolism, Australia

HAYTOĞLU, ZELİHA Et Al. "Lipin1deficiency: A novel mutation in a patient with recurrent habdomyolysis," XIV International Congress of Inborn Errors of Metabolism, Australia, 2021

HAYTOĞLU, ZELİHA Et Al. "Lipin1deficiency: A novel mutation in a patient with recurrent habdomyolysis." XIV International Congress of Inborn Errors of Metabolism , Australia, 2021

HAYTOĞLU, Z. Et Al. (2021) . "Lipin1deficiency: A novel mutation in a patient with recurrent habdomyolysis." XIV International Congress of Inborn Errors of Metabolism , Australia.

@conferencepaper{conferencepaper, author={ZELİHA HAYTOĞLU Et Al. }, title={Lipin1deficiency: A novel mutation in a patient with recurrent habdomyolysis}, congress name={XIV International Congress of Inborn Errors of Metabolism}, city={}, country={Australia}, year={2021}}