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References from A Homozygous Frameshift Variant in KHDC4 Is Associated With a Syndromic Inherited Retinal Disease in Humans. Local targets link to admitted publications; unresolved targets remain external evidence.
10.1016/j.preteyeres.2021.101029
10.1016/j.preteyeres.2021.101029 · External reference
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10.1101/cshperspect.a041277 · External reference
10.1016/j.ajhg.2025.08.017
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10.1074/jbc.m109.036632
10.1074/jbc.m109.036632 · External reference
10.1371/journal.pone.0047497
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10.1016/j.molcel.2024.05.028
10.1016/j.molcel.2024.05.028 · External reference
10.1016/s0968-0004(98)01208-0
10.1016/s0968-0004(98)01208-0 · External reference
10.1093/gigascience/giab061
10.1093/gigascience/giab061 · External reference
10.1074/jbc.m807017200
10.1074/jbc.m807017200 · External reference
10.1038/gim.2015.30
10.1038/gim.2015.30 · External reference
10.1016/j.tig.2023.04.008
10.1016/j.tig.2023.04.008 · External reference
10.1101/cshperspect.a003707
10.1101/cshperspect.a003707 · External reference
10.1038/s41576-022-00556-8
10.1038/s41576-022-00556-8 · External reference
Pre‐mRNA Processing Factors and Retinitis Pigmentosa: RNA Splicing and Beyond
2021 · External reference
10.1167/iovs.07-1483
10.1167/iovs.07-1483 · External reference
10.1093/hmg/ddv073
10.1093/hmg/ddv073 · External reference
10.1001/jamaophthalmol.2024.3836
10.1001/jamaophthalmol.2024.3836 · External reference
