PRRT2 mutations lead to neuronal dysfunction and neurodevelopmental defects-Reference-Cited by-同舟云学术

PRRT2 mutations lead to neuronal dysfunction and neurodevelopmental defects

Published:2016-05-09 Issue:26 Volume:7 Page:39184-39196
ISSN:1949-2553
Container-title:Oncotarget
language:en
Short-container-title:Oncotarget

Author:

Liu Yo-Tsen¹²,Nian Fang-Shin³⁴,Chou Wan-Ju⁴,Tai Chin-Yin⁵,Kwan Shang-Yeong¹²,Chen Chien¹²,Kuo Pei-Wen⁴,Lin Po-Hsi²,Chen Chin-Yi⁶,Huang Chia-Wei⁴,Lee Yi-Chung¹²⁷,Soong Bing-Wen¹²⁷,Tsai Jin-Wu⁴⁷⁸

Affiliation:

1. Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan

2. Department of Neurology, National Yang-Ming University School of Medicine, Taipei, Taiwan

3. Program in Molecular Medicine, National Yang-Ming University and Academia Sinica, Taipei, Taiwan

4. Institute of Brain Science, National Yang-Ming University, Taipei, Taiwan

5. Istitute of Pharmaceutics, Development Center for Biotechnology, New Taipei City, Taiwan

6. Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan

7. Brain Research Center, National Yang-Ming University, Taipei, Taiwan

8. Biophotonics and Molecular Imaging Research Center, National Yang-Ming University, Taipei, Taiwan

Publisher

Impact Journals, LLC

Subject

Oncology

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