Cite
HARVARD Citation
Guen, V. et al. (2018). A homozygous deleterious CDK10 mutation in a patient with agenesis of corpus callosum, retinopathy, and deafness. American journal of medical genetics. 176 (1), pp. 92-98. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Guen, V. et al. (2018). A homozygous deleterious CDK10 mutation in a patient with agenesis of corpus callosum, retinopathy, and deafness. American journal of medical genetics. 176 (1), pp. 92-98. [Online].