A Segmental Copy Number Loss of the SFMBT1 Gene Is a Genetic Risk for Shunt-Responsive, Idiopathic Normal Pressure Hydrocephalus (iNPH): A Case-Control Study
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Title
A Segmental Copy Number Loss of the SFMBT1 Gene Is a Genetic Risk for Shunt-Responsive, Idiopathic Normal Pressure Hydrocephalus (iNPH): A Case-Control Study
Authors
Keywords
Introns, Human genetics, Parkinson disease, Elderly, Geriatrics, Magnetic resonance imaging, Genetic predisposition, Polymerase chain reaction
Journal
PLoS One
Volume 11, Issue 11, Pages e0166615
Publisher
Public Library of Science (PLoS)
Online
2016-11-19
DOI
10.1371/journal.pone.0166615
References
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Note: Only part of the references are listed.- Lumboperitoneal shunt surgery for idiopathic normal pressure hydrocephalus (SINPHONI-2): an open-label randomised trial
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