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Article

Copy number loss in SFMBT1 is common among Finnish and Norwegian patients with iNPH

1 Dec 2018

Abstract excerpt

Objective To evaluate the role of the copy number loss in SFMBT1 in a Caucasian population. Methods Five hundred sixty-seven Finnish and 377 Norwegian patients with idiopathic normal pressure hydrocephalus (iNPH) were genotyped and compared with 508 Finnish elderly, neurologically healthy controls. The copy number loss in intron 2 of SFMBT1 was determined using quantitative PCR. Results The copy number loss in...

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PMID: 30584596
DOI: 10.1212/nxg.0000000000000291

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