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

Little is known about genetic risk factors for idiopathic normal pressure hydrocephalus (iNPH). We examined whether a copy number loss in intron 2 of the SFMBT1 gene could be a genetic risk for shunt-responsive, definite iNPH. Quantitative and digital PCR analyses revealed that 26.0% of shunt-respon...

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Vydáno v:PLoS One
Hlavní autoři: Sato, Hidenori, Takahashi, Yoshimi, Kimihira, Luna, Iseki, Chifumi, Kato, Hajime, Suzuki, Yuya, Igari, Ryosuke, Sato, Hiroyasu, Koyama, Shingo, Arawaka, Shigeki, Kawanami, Toru, Miyajima, Masakazu, Samejima, Naoyuki, Sato, Shinya, Kameda, Masahiro, Yamada, Shinya, Kita, Daisuke, Kaijima, Mitsunobu, Date, Isao, Sonoda, Yukihiko, Kayama, Takamasa, Kuwana, Nobumasa, Arai, Hajime, Kato, Takeo
Médium: Artigo
Jazyk:Inglês
Vydáno: Public Library of Science 2016
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5115754/
https://ncbi.nlm.nih.gov/pubmed/27861535
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0166615
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