@article{6d5cd58f4efb454fb7f24dc50db3976c,
title = "VMAT1 deletion causes neuronal loss in the hippocampus and neurocognitive deficits in spatial discrimination",
keywords = "Apoptosis, Cognition, Hippocampus, Neurogenesis, SLC18A1",
author = "Multani, \{P. K.\} and R. Hodge and Est{\'e}vez, \{M. A.\} and T. Abel and H. Kung and M. Alter and B. Brookshire and I. Lucki and Nall, \{A. H.\} and K. Talbot and Doyle, \{G. A.\} and Lohoff, \{F. W.\}",
note = "Funding Information: This work was supported by the Center for Neurobiology and Behavior, Department of Psychiatry, University of Pennsylvania. Financial support is gratefully acknowledged from National Institutes of Health Grants NIH K08MH080372 (F.W.L.), R01MH86599 (I.L.) and T32MH14654 (B.B.). We thank Raymond Meade for assistance with electron microscopy experiments, Seok Rye Choi for help with the biodistribution experiments and Tiffany Smith for technical assistance. Dr. Kung declares that he is named as one of the inventors of a patent involving AV-133. Dr. Lohoff declares that he is named as one of the inventors of a patent (assigned to the University of Pennsylvania) involving human genetic VMAT1 variants (U.S. Pat. No. 7,736,852).",
year = "2013",
month = mar,
day = "1",
doi = "10.1016/j.neuroscience.2012.11.023",
language = "English",
volume = "232",
pages = "32--44",
journal = "Neuroscience",
issn = "0306-4522",
}