A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant.
| Autor: | Uddin, Mohammed Shahab1 dr.mshahabu@gmail.com, Alradhi, AlZahra Y.1, Alqathani, Fahad Mushbb N.1, Alessa, Othman Saleh1, Alshammari, Ahmed Nawfal M.1, Tripathy, Ratna2, Alomari, Mohammed Ahmed1 |
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| Zdroj: | American Journal of Case Reports. 3/26/2024, Vol. 25, p1-10. 10p. |
| Databáze: | Academic Search Ultimate |
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