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Coat’s like vasculopathy in leber congenital amaurosis secondary to homozygous mutations in CRB1: a case report and discussion of the management options

Crossref DOI link: https://doi.org/10.1186/s13104-016-1917-6

Published Online: 2016-02-13

Published Print: 2016-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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