Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, a Gene Implicated in Ubiquitination

Overview of attention for article published in American Journal of Human Genetics, August 2016

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Another article in which pxlence assays were used for targeted resequencing https://t.co/LZXOIYrtjg

RT @varsome: Mutations https://t.co/qy6GIuzfgw https://t.co/uTRBoVDSTL cause autosomal-recessive Isolated Retinal Dystrophy @AJHG https://t…

Mutations https://t.co/qy6GIuzfgw https://t.co/uTRBoVDSTL cause autosomal-recessive Isolated Retinal Dystrophy @AJHG https://t.co/5uliBAvqNa

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