APA (7th ed.) Citation

Liangshan Li, Liangshan Li, Xiangmao Bu, Yuhua Ji, Ping Tan, & Shiguo Liu. (2021). A Novel Homozygous VPS13B Splice-Site Mutation Causing the Skipping of Exon 38 in a Chinese Family With Cohen Syndrome. Frontiers Media S.A..

Chicago Style (17th ed.) Citation

Liangshan Li, Liangshan Li, Xiangmao Bu, Yuhua Ji, Ping Tan, and Shiguo Liu. A Novel Homozygous VPS13B Splice-Site Mutation Causing the Skipping of Exon 38 in a Chinese Family With Cohen Syndrome. Frontiers Media S.A., 2021.

MLA (9th ed.) Citation

Liangshan Li, et al. A Novel Homozygous VPS13B Splice-Site Mutation Causing the Skipping of Exon 38 in a Chinese Family With Cohen Syndrome. Frontiers Media S.A., 2021.