Yücel, H. Et Al. 2021. Treatment difficulties in hypomagnesemia secondary to the transient receptor potential melastatin 6 gene: A case report with novel mutation. JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.13, no.1 , 114-118.

Yücel, H., Sel, Ç. G., Kasapkara, Ç. S., Küçükali, G. K., Savas-Erdeve, S., Öztoprak, Ü., ... CEYLANER, S.(2021). Treatment difficulties in hypomagnesemia secondary to the transient receptor potential melastatin 6 gene: A case report with novel mutation. JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.13, no.1, 114-118.

Yücel, Hüsniye Et Al. "Treatment difficulties in hypomagnesemia secondary to the transient receptor potential melastatin 6 gene: A case report with novel mutation," JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.13, no.1, 114-118, 2021

Yücel, Hüsniye Et Al. "Treatment difficulties in hypomagnesemia secondary to the transient receptor potential melastatin 6 gene: A case report with novel mutation." JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.13, no.1, pp.114-118, 2021

Yücel, H. Et Al. (2021) . "Treatment difficulties in hypomagnesemia secondary to the transient receptor potential melastatin 6 gene: A case report with novel mutation." JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.13, no.1, pp.114-118.

@article{article, author={Hüsniye Yücel Et Al. }, title={Treatment difficulties in hypomagnesemia secondary to the transient receptor potential melastatin 6 gene: A case report with novel mutation}, journal={JCRPE Journal of Clinical Research in Pediatric Endocrinology}, year=2021, pages={114-118} }