The p.(Gly111Arg) ABCC8 Variant: A Founder Mutation Causing Congenital Hyperinsulinism in the Indian Agarwal Community.

MLA

Jain, Vandana, et al. “The p.(Gly111Arg) ABCC8 Variant: A Founder Mutation Causing Congenital Hyperinsulinism in the Indian Agarwal Community.” Clinical Genetics, vol. 107, no. 3, Mar. 2025, pp. 364–65. EBSCOhost, https://doi.org/10.1111/cge.14657.

APA

Jain, V., Radha, V., Mohan, V., Wakeling, M. N., Bennett, J. J., & Flanagan, S. E. (2025). The p.(Gly111Arg) ABCC8 Variant: A Founder Mutation Causing Congenital Hyperinsulinism in the Indian Agarwal Community. Clinical Genetics, 107(3), 364–365. https://doi.org/10.1111/cge.14657

Chicago

Jain, Vandana, Venkatesan Radha, Viswanathan Mohan, Matthew N Wakeling, Jasmin J Bennett, and Sarah E Flanagan. 2025. “The p.(Gly111Arg) ABCC8 Variant: A Founder Mutation Causing Congenital Hyperinsulinism in the Indian Agarwal Community.” Clinical Genetics 107 (3): 364–65. doi:10.1111/cge.14657.