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Paper Details

Rare occult macular dystrophy with a pathogenic variant in the RP1L1 gene in a patient of Swiss descent.
Am J Ophthalmol Case Rep
0
2022
Author NameAffiliation
Hendrik P N SchollUniversity of Basel
Hendrik P N SchollInstitute of Molecular and Clinical Ophthalmology Basel (IOB)
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Datasets

Release 1.2