एपीए उद्धरण

Karimi, A. H., Karimi, M. R., Farnia, P., Parvini, F., & Foroutan, M. (2020). A Homozygous Truncating Mutation in NALCN Causing IHPRF1: Detailed Clinical Manifestations and a Review of Literature. Appl Clin Genet.

शिकागो स्टाइल उद्धरण

Karimi, Amir Hossein, Mohammad Reza Karimi, Poopak Farnia, Farshid Parvini, और Majid Foroutan. "A Homozygous Truncating Mutation in NALCN Causing IHPRF1: Detailed Clinical Manifestations and a Review of Literature." Appl Clin Genet 2020.

एमएलए उद्धरण

Karimi, Amir Hossein, et al. "A Homozygous Truncating Mutation in NALCN Causing IHPRF1: Detailed Clinical Manifestations and a Review of Literature." Appl Clin Genet 2020.