P. TEKE KISA Et Al. , "Clinical and molecular characterization of cerebtendinous xanthomatosis: case series," Society for the study of Inborn Error of Metabolism. , vol.42, Rotterdam, Netherlands, pp.216, 2019
TEKE KISA, P. Et Al. 2019. Clinical and molecular characterization of cerebtendinous xanthomatosis: case series. Society for the study of Inborn Error of Metabolism. , (Rotterdam, Netherlands), 216.
TEKE KISA, P., ÖZTÜRK HİŞMİ, B., Gülten Arslan, z., Yılmaz Kusbeci, Ö., YAMAN, A., & ARSLAN, N., (2019). Clinical and molecular characterization of cerebtendinous xanthomatosis: case series . Society for the study of Inborn Error of Metabolism. (pp.216). Rotterdam, Netherlands
TEKE KISA, PELİN Et Al. "Clinical and molecular characterization of cerebtendinous xanthomatosis: case series," Society for the study of Inborn Error of Metabolism., Rotterdam, Netherlands, 2019
TEKE KISA, PELİN T. Et Al. "Clinical and molecular characterization of cerebtendinous xanthomatosis: case series." Society for the study of Inborn Error of Metabolism. , Rotterdam, Netherlands, pp.216, 2019
TEKE KISA, P. Et Al. (2019) . "Clinical and molecular characterization of cerebtendinous xanthomatosis: case series." Society for the study of Inborn Error of Metabolism. , Rotterdam, Netherlands, p.216.
@conferencepaper{conferencepaper, author={PELİN TEKE KISA Et Al. }, title={Clinical and molecular characterization of cerebtendinous xanthomatosis: case series}, congress name={Society for the study of Inborn Error of Metabolism.}, city={Rotterdam}, country={Netherlands}, year={2019}, pages={216} }