Discovery of a neuromuscular syndrome caused by biallelic variants in ASCC3

Overview of attention for article published in Human Genetics and Genomics Advances, January 2021

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RT @CellPressNews: Access a report from @HGGAdvances: Discovery of a neuromuscular syndrome caused by biallelic variants in ASCC3 @Genetics…

Access a report from @HGGAdvances: Discovery of a neuromuscular syndrome caused by biallelic variants in ASCC3 @GeneticsSociety @Ebhoj https://t.co/jEoouJ0p6X https://t.co/0BdeKPUzDj

RT @EBhoj: Congrats to Divya Nair, PGY1 peds-genetics at CHOP, for leading this new syndrome discovery!

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