PT604. Attenuation of PTZ-induced epileptic seizure by deficiency in the gene encoding solute carrier OCTN1/SLC22A4

Detalles Bibliográficos
Autores principales: Nakamichi, Noritaka, Kato, Yukio, Masuo, Yusuke, Nishiyama, Misa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Abstracts
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5616937/
http://dx.doi.org/10.1093/ijnp/pyw044.604
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author Nakamichi, Noritaka
Kato, Yukio
Masuo, Yusuke
Nishiyama, Misa
author_facet Nakamichi, Noritaka
Kato, Yukio
Masuo, Yusuke
Nishiyama, Misa
author_sort Nakamichi, Noritaka
collection PubMed
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spelling pubmed-56169372017-11-27 PT604. Attenuation of PTZ-induced epileptic seizure by deficiency in the gene encoding solute carrier OCTN1/SLC22A4 Nakamichi, Noritaka Kato, Yukio Masuo, Yusuke Nishiyama, Misa Int J Neuropsychopharmacol Abstracts Oxford University Press 2016-05-27 /pmc/articles/PMC5616937/ http://dx.doi.org/10.1093/ijnp/pyw044.604 Text en © The Author 2016. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.
spellingShingle Abstracts
Nakamichi, Noritaka
Kato, Yukio
Masuo, Yusuke
Nishiyama, Misa
PT604. Attenuation of PTZ-induced epileptic seizure by deficiency in the gene encoding solute carrier OCTN1/SLC22A4
title PT604. Attenuation of PTZ-induced epileptic seizure by deficiency in the gene encoding solute carrier OCTN1/SLC22A4
title_full PT604. Attenuation of PTZ-induced epileptic seizure by deficiency in the gene encoding solute carrier OCTN1/SLC22A4
title_fullStr PT604. Attenuation of PTZ-induced epileptic seizure by deficiency in the gene encoding solute carrier OCTN1/SLC22A4
title_full_unstemmed PT604. Attenuation of PTZ-induced epileptic seizure by deficiency in the gene encoding solute carrier OCTN1/SLC22A4
title_short PT604. Attenuation of PTZ-induced epileptic seizure by deficiency in the gene encoding solute carrier OCTN1/SLC22A4
title_sort pt604. attenuation of ptz-induced epileptic seizure by deficiency in the gene encoding solute carrier octn1/slc22a4
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5616937/
http://dx.doi.org/10.1093/ijnp/pyw044.604
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