Case Report: A novel mutation in WFS1 gene (c.1756G>A p.A586T) is responsible for early clinical features of cognitive impairment and recurrent ischemic stroke

Overview of attention for article published in Frontiers in Genetics, February 2023

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New Research: Case Report: A novel mutation in WFS1 gene (c.1756G>A p.A586T) is responsible for early clinical features of cognitive impairment and recurrent ischemic stroke: Wolfram syndrome 1 (WFS1) gene mutations can be dominantly or… https://t.co/7f

02 Feb 2023

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