Copy number loss in <i>SFMBT1</i> is common among Finnish and Norwegian patients with iNPH

Abstract

This is the largest and the first multinational study reporting the increased prevalence of the copy number loss in intron 2 of <i>SFMBT1</i> among patients with iNPH, providing further evidence of its role in iNPH. The pathogenic role still remains unclear, requiring further study.