Cite
HARVARD Citation
Sha, Y. et al. (2020). Loss‐of‐function mutations in centrosomal protein 112 is associated with human acephalic spermatozoa phenotype. Clinical genetics. 97 (2), pp. 321-328. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Sha, Y. et al. (2020). Loss‐of‐function mutations in centrosomal protein 112 is associated with human acephalic spermatozoa phenotype. Clinical genetics. 97 (2), pp. 321-328. [Online].