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

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Description scientific article published on 31 October 2018
Author/s

author: Frauke Coppieters  Marta Cortón  Annalaura Torella  Stijn Van de Sompele  Claire E. L. Smith  Julie De Zaeytijd  Bart Leroy 

Publication date October 31, 2018
Language English
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