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

Abstract

OBJECTIVE: in a Caucasian population. METHODS: was determined using quantitative PCR. RESULTS: copy number loss carriers and noncarriers. CONCLUSIONS: among patients with iNPH, providing further evidence of its role in iNPH. The pathogenic role still remains unclear, requiring further study.