Copy number loss in SFMBT1 is common among Finnish and Norwegian patients with iNPH.
Neurol Genet. 2018 Dec 3;4(6):e291. doi: 10.1212/NXG.0000000000000291. eCollection 2018 Dec.
Neurol Genet. 2018.
PMID: 30584596
Free PMC article.