Cite
HARVARD Citation
Ramadesikan, S. et al. (2021). Genotype & phenotype in Lowe Syndrome: specific OCRL1 patient mutations differentially impact cellular phenotypes. Human molecular genetics. 30 (3), pp. 198-212. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Ramadesikan, S. et al. (2021). Genotype & phenotype in Lowe Syndrome: specific OCRL1 patient mutations differentially impact cellular phenotypes. Human molecular genetics. 30 (3), pp. 198-212. [Online].