Associated Papers
Screening copy number variations in 35 unsolved inherited retinal disease families.
Liu X et al.
Human Genetics, 2024
Mutation Spectrum of the ABCA4 Gene in a Greek Cohort with Stargardt Disease: Identification of Novel Mutations and Evidence of Three Prevalent Mutated Alleles.
Smaragda K et al.
Journal of Ophthalmology, 2018
29854428 (PubMed )
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