Identification of rare missense variants reducing cathepsin O secretion in families with intracranial aneurysmMilène Fréneau(Centre National de la Recherche Scientifique), Richard Redon(Centre National de la Recherche Scientifique)medRxivFebruary 2, 202310.1101/2023.01.31.23285168Cited by 0SaveCiteExport RISWatch citationsRelated PapersOrigins and functional impact of copy number variation in the human genome|Nature|2009|2kGenome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls|Nature|2010|812