Bart Peter Leroy
0000-0002-9899-2081
Children's Hospital of Philadelphia
4 papers found
Refreshing results…
Fleck-like lesions in CEP290-associated leber congenital amaurosis: a case series
Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy
Intravitreal antisense oligonucleotide sepofarsen in Leber congenital amaurosis type 10: a phase 1b/2 trial
Functional characterization of the first missense variant in CEP78 , a founder allele associated with cone‐rod dystrophy, hearing loss, and reduced male fertility
Missing publications? Search for publications with a matching author name.