Cite
HARVARD Citation
Gradstein, L. et al. (2016). Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred. BMC medical genetics. 17 (1), pp. 1-6. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Gradstein, L. et al. (2016). Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred. BMC medical genetics. 17 (1), pp. 1-6. [Online].