Turkmen, M. O. Et Al. 2021. Functional analyses of three different mutations in the AVP-NPII gene causing familial neurohypophyseal diabetes insipidus. ENDOCRINE , vol.74, no.3 , 658-665.

Turkmen, M. O., Karaduman, T., ERDEM TUNÇDEMİR, B., ÜNAL, M. A., & MERGEN, H., (2021). Functional analyses of three different mutations in the AVP-NPII gene causing familial neurohypophyseal diabetes insipidus. ENDOCRINE , vol.74, no.3, 658-665.

Turkmen, Merve Et Al. "Functional analyses of three different mutations in the AVP-NPII gene causing familial neurohypophyseal diabetes insipidus," ENDOCRINE , vol.74, no.3, 658-665, 2021

Turkmen, Merve O. Et Al. "Functional analyses of three different mutations in the AVP-NPII gene causing familial neurohypophyseal diabetes insipidus." ENDOCRINE , vol.74, no.3, pp.658-665, 2021

Turkmen, M. O. Et Al. (2021) . "Functional analyses of three different mutations in the AVP-NPII gene causing familial neurohypophyseal diabetes insipidus." ENDOCRINE , vol.74, no.3, pp.658-665.

@article{article, author={Merve Ozcan Turkmen Et Al. }, title={Functional analyses of three different mutations in the AVP-NPII gene causing familial neurohypophyseal diabetes insipidus}, journal={ENDOCRINE}, year=2021, pages={658-665} }