APA (7th ed.) Citation

Chandreyee Bhattacharya, Rajiv Sinha, Subrata Dey, & Kaushik Maulik. (2024). A Rare Compound Heterozygous Mutation of TRPM6 Gene in Hereditary Hypomagnesemia with Secondary Hypocalcemia: A Cause of Refractory Seizures in an Infant. Wolters Kluwer Medknow Publications.

Chicago Style (17th ed.) Citation

Chandreyee Bhattacharya, Rajiv Sinha, Subrata Dey, and Kaushik Maulik. A Rare Compound Heterozygous Mutation of TRPM6 Gene in Hereditary Hypomagnesemia with Secondary Hypocalcemia: A Cause of Refractory Seizures in an Infant. Wolters Kluwer Medknow Publications, 2024.

MLA (9th ed.) Citation

Chandreyee Bhattacharya, et al. A Rare Compound Heterozygous Mutation of TRPM6 Gene in Hereditary Hypomagnesemia with Secondary Hypocalcemia: A Cause of Refractory Seizures in an Infant. Wolters Kluwer Medknow Publications, 2024.