A novel mutation in RS1 and clinical manifestations in a Chinese twin family with congenital retinoschisis

Overview of attention for article published in Frontiers in Genetics, September 2022

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A novel mutation in RS1 and clinical manifestations in a Chinese twin family with congenital retinoschisis https://t.co/kcxJ0OOTEs https://t.co/SBXAMgzKzD

15 Oct 2022

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New Research: A novel mutation in RS1 and clinical manifestations in a Chinese twin family with congenital retinoschisis: Purpose: We aim to analyze the clinical and genetic features in a Chinese family with congenital retinoschisis by… https://t.co/rrxvIT

23 Sep 2022

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