Associated Papers
Dominant RP in the Middle While Recessive in Both the N- and C-Terminals Due to RP1 Truncations: Confirmation, Refinement, and Questions.
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Supplement: Table_4.XLSX › Sheet1
Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.
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Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families.
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Plos One, 2017
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