Eltan, M. Et Al. 2022. Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features. CALCIFIED TISSUE INTERNATIONAL , vol.110, no.4 , 441-450.

Eltan, M., Abali, Z. Y., Turkyilmaz, A., Gökce, İ., Abali, S., Alavanda, C., ... Arman, A.(2022). Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features. CALCIFIED TISSUE INTERNATIONAL , vol.110, no.4, 441-450.

Eltan, MEHMET Et Al. "Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features," CALCIFIED TISSUE INTERNATIONAL , vol.110, no.4, 441-450, 2022

Eltan, MEHMET Et Al. "Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features." CALCIFIED TISSUE INTERNATIONAL , vol.110, no.4, pp.441-450, 2022

Eltan, M. Et Al. (2022) . "Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features." CALCIFIED TISSUE INTERNATIONAL , vol.110, no.4, pp.441-450.

@article{article, author={MEHMET ELTAN Et Al. }, title={Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features}, journal={CALCIFIED TISSUE INTERNATIONAL}, year=2022, pages={441-450} }