De Novo Coding Variants Are Strongly Associated with Tourette Disorder.
about
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.Editorial: The Neurobiology and Genetics of Gilles de la Tourette Syndrome: New Avenues through Large-Scale Collaborative ProjectsTourette syndrome: a disorder of the social decision-making network.Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.Progress in Genetic Studies of Tourette's Syndrome.Psychiatric genetics and the structure of psychopathology.The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family.Distinctive phosphoinositide and Ca2+ binding properties of normal and cognitive performance-linked variant forms of KIBRA C2 domain.Many genes involved in Tourette syndrome pathogenesis.
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P2860
De Novo Coding Variants Are Strongly Associated with Tourette Disorder.
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
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2017年学术文章
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name
De Novo Coding Variants Are Strongly Associated with Tourette Disorder.
@en
De Novo Coding Variants Are Strongly Associated with Tourette Disorder.
@nl
type
label
De Novo Coding Variants Are Strongly Associated with Tourette Disorder.
@en
De Novo Coding Variants Are Strongly Associated with Tourette Disorder.
@nl
prefLabel
De Novo Coding Variants Are Strongly Associated with Tourette Disorder.
@en
De Novo Coding Variants Are Strongly Associated with Tourette Disorder.
@nl
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P2860
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De Novo Coding Variants Are Strongly Associated with Tourette Disorder.
@en
P2093
A Jeremy Willsey
Alden Y Huang
Andrea Dietrich
Benjamin M Neale
Carol A Mathews
Giovanni Coppola
Jeffrey D Mandell
Jeremiah M Scharf
Jinchuan Xing
Louw Smith
P2860
P304
486-499.e9
P356
10.1016/J.NEURON.2017.04.024
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P577
2017-05-01T00:00:00Z