He, X., Liu, C., Yang, X., Lv, M., Ni, X., Li, Q., . . . Cao, Y. (2020). Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice. Am J Hum Genet.
Stile di citazione ChicagoHe, Xiaojin, et al. "Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice." Am J Hum Genet 2020.
Citazione MLAHe, Xiaojin, et al. "Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice." Am J Hum Genet 2020.
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