A Dominant Heterozygous Mutation in COG4 Causes Saul–Wilson Syndrome, a Primordial Dwarfism, and Disrupts Zebrafish Development via Wnt Signaling

Overview of attention for article published in Frontiers in Cell and Developmental Biology, September 2021

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A Dominant Heterozygous Mutation in COG4 Causes Saul-Wilson Syndrome, a Primordial Dwarfism, and Disrupts Zebrafish Development via Wnt Signaling https://t.co/Am07zUwYd3

01 Oct 2021

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New Research: A Dominant Heterozygous Mutation in COG4 Causes Saul–Wilson Syndrome, a Primordial Dwarfism, and Disrupts Zebrafish Development via Wnt Signaling: Saul–Wilson syndrome (SWS) is a rare, skeletal dysplasia with progeroid… https://t.co/avdkrgHAw

16 Sep 2021

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