Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred
Crossref DOI link:
Published Online: 2016-07-30
Published Print: 2016-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Sergeev, Yuri V.
Birk, Ohad S.
Funding for this research was provided by:
Israeli Ministry of Health Research Grant (3-11799)
Kahn Family Foundation