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WFS1 #mutations https://t.co/kHLlwCVMCC in 13 #Iranian families with #Wolfram syndrome #diabetes mellitus, #optic nerve atrophy, sensorineural #hearingloss and urinary tract abnormalities #genetics https://t.co/88VpcsjCgz
WFS1 #mutations https://t.co/kHLlwCVMCC in 13 #Iranian families with #Wolfram syndrome #diabetes mellitus, #optic nerve atrophy, sensorineural #hearingloss and urinary tract abnormalities #genetics https://t.co/88VpcsjCgz
Clinical and molecular assessment of 13 Iranian families with Wolfram syndrome. https://t.co/AtonT8I5EO