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Items: 5

1.
An autism-causing calcium channel variant functions with selective autophagy to alter axon targeting and behavior
Tyler Buddell, Vladislav Friedman, Cody J. Drozd, Christopher C. Quinn
PLoS Genet. 2019 Dec; 15(12): e1008488. Published online 2019 Dec 5. doi: 10.1371/journal.pgen.1008488
PMCID:
PMC6894750
AbstractArticlePDF–1.4M
2.
Identification of a novel mutation in the CACNA1C gene in a Chinese family with autosomal dominant cerebellar ataxia
Jiajun Chen, Yajuan Sun, Xiaoyang Liu, Jia Li
BMC Neurol. 2019; 19: 157. Published online 2019 Jul 10. doi: 10.1186/s12883-019-1381-8
PMCID:
PMC6617910
AbstractArticlePDF–755K
3.
CACNA1C (rs1006737) may be a susceptibility gene for schizophrenia: An updated meta‐analysis
Dongjian Zhu, Jingwen Yin, Chunmei Liang, Xudong Luo, Dong Lv, Zhun Dai, Susu Xiong, Jiawu Fu, You Li, Juda Lin, Zhixiong Lin, Yajun Wang, Guoda Ma
Brain Behav. 2019 Jun; 9(6): e01292. Published online 2019 Apr 29. doi: 10.1002/brb3.1292
PMCID:
PMC6576147
AbstractArticlePDF–1.8M
4.
CACNA1C Polymorphism (rs2283291) Is Associated with Schizophrenia in Chinese Males: A Case-Control Study
Xiaojing Zhu, Rixin Li, Guojun Kang, Qi Kang, Wenwang Rao, Mingjia Yang, Bonan Cao, Mingyuan Zhang, Yaoyao Sun, Yueying Wang, Xin Chen, Yaqin Yu, Qiong Yu
Dis Markers. 2019; 2019: 8062397. Published online 2019 Apr 1. doi: 10.1155/2019/8062397
PMCID:
PMC6466926
AbstractArticlePDF–691K
5.
Molecular diversity of L-type Ca2+ channel transcripts in human fibroblasts.
N M Soldatov
Proc Natl Acad Sci U S A. 1992 May 15; 89(10): 4628–4632. doi: 10.1073/pnas.89.10.4628
PMCID:
PMC49136
SummaryPage BrowsePDF–1.3M

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