Endolymphatic Hydrop Phenotype in Familial Norrie Disease Caused by Large Fragment Deletion of NDP

Overview of attention for article published in Frontiers in Aging Neuroscience, April 2022

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Endolymphatic Hydrop Phenotype in Familial Norrie Disease Caused by Large Fragment Deletion of NDP https://t.co/GTIpMkTHe8 https://t.co/0LuSyhQXAy

06 May 2022

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New Research: Endolymphatic Hydrop Phenotype in Familial Norrie Disease Caused by Large Fragment Deletion of NDP: Norrie disease (ND; OMIM 310600), a rare X-linked recessive genetic disorder, is characterized by congenital blindness… https://t.co/gXPyXMAd1

30 Apr 2022

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