Clinical and molecular investigation of 37 Japanese patients with multiple acyl-CoA dehydrogenase deficiency: p.Y507D in ETFDH , a common Japanese variant, causes a mortal phenotype.

MLA

Yamada, Kenji, et al. “Clinical and Molecular Investigation of 37 Japanese Patients with Multiple Acyl-CoA Dehydrogenase Deficiency: P.Y507D in ETFDH , a Common Japanese Variant, Causes a Mortal Phenotype.” Molecular Genetics and Metabolism Reports, vol. 33, Nov. 2022, p. 100940. EBSCOhost, https://doi.org/10.1016/j.ymgmr.2022.100940.

APA

Yamada, K., Osawa, Y., Kobayashi, H., Bo, R., Mushimoto, Y., Hasegawa, Y., Yamaguchi, S., & Taketani, T. (2022). Clinical and molecular investigation of 37 Japanese patients with multiple acyl-CoA dehydrogenase deficiency: p.Y507D in ETFDH , a common Japanese variant, causes a mortal phenotype. Molecular Genetics and Metabolism Reports, 33, 100940. https://doi.org/10.1016/j.ymgmr.2022.100940

Chicago

Yamada, Kenji, Yoshimitsu Osawa, Hironori Kobayashi, Ryosuke Bo, Yuichi Mushimoto, Yuki Hasegawa, Seiji Yamaguchi, and Takeshi Taketani. 2022. “Clinical and Molecular Investigation of 37 Japanese Patients with Multiple Acyl-CoA Dehydrogenase Deficiency: P.Y507D in ETFDH , a Common Japanese Variant, Causes a Mortal Phenotype.” Molecular Genetics and Metabolism Reports 33 (November): 100940. doi:10.1016/j.ymgmr.2022.100940.