Search Results - Alqathani, Fahad Mushbb N.

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    A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant

    A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant by Uddin, Mohammed Shahab, Alradhi, AlZahra Y, Alqathani, Fahad Mushbb N, Alessa, Othman Saleh, Alshammari, Ahmed Nawfal M, Tripathy, Ratna, Alomari, Mohammed Ahmed

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    A 26-Day-Old Neonate Presenting with Familial Hypomagnesemia with Secondary Hypocalcemia Associated with the Novel Homozygous TRPM6 Gene Variant c.5281C>G p. (Arg1761Gly) chr9: 77354845 – A Case Report

    A 26-Day-Old Neonate Presenting with Familial Hypomagnesemia with Secondary Hypocalcemia Associated with the Novel Homozygous TRPM6 Gene Variant c.5281C>G p. (Arg1761Gly) chr9: 773... by Uddin, Mohammed Shahab, Alradhi, AlZahra Y., Alqathani, Fahad Mushbb N., Alessa, Othman Saleh, Alshammari, Ahmed Nawfal M., Tripathy, Ratna, Alomari, Mohammed Ahmed

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