Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease

Overview of attention for article published in Genetics in Medicine, October 2018

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RT @elfridedebaere: Our newest paper in @GIMJournal online, resulting from joint efforts of four teams of the European Retinal Disease Cons…

Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease. https://t.co/0Am4HBH1XW https://t.co/5Q9YHRGUYO

RT @elfridedebaere: Our newest paper in @GIMJournal online, resulting from joint efforts of four teams of the European Retinal Disease Cons…

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