APA (7th ed.) Citation

Wei-De Lin, Fuu-Jen Tsai, & Chung-Hsing Wang. (2023). Identification of a novel deletion mutation in PHKA2 in a taiwanese patient with type IXa glycogen storage disease. Elsevier.

Chicago Style (17th ed.) Citation

Wei-De Lin, Fuu-Jen Tsai, and Chung-Hsing Wang. Identification of a Novel Deletion Mutation in PHKA2 in a Taiwanese Patient with Type IXa Glycogen Storage Disease. Elsevier, 2023.

MLA (9th ed.) Citation

Wei-De Lin, et al. Identification of a Novel Deletion Mutation in PHKA2 in a Taiwanese Patient with Type IXa Glycogen Storage Disease. Elsevier, 2023.