Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
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Editorial: The Neurobiology and Genetics of Gilles de la Tourette Syndrome: New Avenues through Large-Scale Collaborative ProjectsTourette syndrome research highlights from 2016.Progress in Genetic Studies of Tourette's Syndrome.Synaptic Neurexin Complexes: A Molecular Code for the Logic of Neural Circuits.Current Approaches and New Developments in the Pharmacological Management of Tourette Syndrome.Allele-Specific Biased Expression of the CNTN6 Gene in iPS Cell-Derived Neurons from a Patient with Intellectual Disability and 3p26.3 Microduplication Involving the CNTN6 Gene.Complex genetics of Tourette's Syndrome: Piecing the puzzle.Cntn6 deficiency impairs allocentric navigation in mice.Transcranial Magnetic Stimulation in Tourette Syndrome: A Historical Perspective, Its Current Use and the Influence of Comorbidities in Treatment ResponseHeparan Sulfate Organizes Neuronal Synapses through Neurexin Partnerships
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P2860
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
description
2017 nî lūn-bûn
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2017年の論文
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2017年論文
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2017年論文
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2017年論文
@zh-hk
2017年論文
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2017年論文
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2017年论文
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2017年论文
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name
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
@en
type
label
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
@en
prefLabel
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
@en
P2093
P2860
P50
P1433
P1476
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
@en
P2093
Alden Y Huang
Anastasios Konstantinidis
Andreas Hartmann
Benjamin M Neale
Carlos N Pato
Carol A Mathews
Cathy L Budman
Cheston Berlin
Christel Depienne
Cornelia Illmann
P2860
P304
1101-1111.e7
P356
10.1016/J.NEURON.2017.06.010
P407
P50
P577
2017-06-01T00:00:00Z