Ye, Y., Wei, X., Sha, Y., Li, N., Yan, X., Cheng, L., . . . Li, Y. (2020). Loss‐of‐function mutation in TSGA10 causes acephalic spermatozoa phenotype in human. Mol Genet Genomic Med.
Chicago Style CitationYe, Yuanyuan, et al. "Loss‐of‐function Mutation in TSGA10 Causes Acephalic Spermatozoa Phenotype in Human." Mol Genet Genomic Med 2020.
Cita MLAYe, Yuanyuan, et al. "Loss‐of‐function Mutation in TSGA10 Causes Acephalic Spermatozoa Phenotype in Human." Mol Genet Genomic Med 2020.
Atenció: Aquestes cites poden no estar 100% correctes.