Emerging Monogenic Complex Hyperkinetic Disorders.

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An Ontology Systems Approach on Human Brain Expression and Metaproteomics.Expression map of 78 brain-expressed mouse orphan GPCRs provides a translational resource for neuropsychiatric research

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Emerging Monogenic Complex Hyperkinetic Disorders.

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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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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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name

Emerging Monogenic Complex Hyperkinetic Disorders.

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Emerging Monogenic Complex Hyperkinetic Disorders.

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Emerging Monogenic Complex Hyperkinetic Disorders.

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Emerging Monogenic Complex Hyperkinetic Disorders.

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Emerging Monogenic Complex Hyperkinetic Disorders.

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Emerging Monogenic Complex Hyperkinetic Disorders.

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P1476

Emerging Monogenic Complex Hyperkinetic Disorders

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P2093

Niccolò E Mencacci

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Creative Commons Attribution 4.0 International

P2860

Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia

Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

FOXG1 is responsible for the congenital variant of Rett syndrome

Deleterious mutation in GPR88 is associated with chorea, speech delay, and learning disabilities.

TBC1D24 genotype-phenotype correlation: Epilepsies and other neurologic features.

Delineation of the movement disorders associated withFOXG1mutations: Table 1

Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy

The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene

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s11910-017-0806-2

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scholarly article

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10.1007/S11910-017-0806-2

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Miryam Carecchio

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2017-10-30T00:00:00Z

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29086067

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movement disorder

genetic variation

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Emerging Monogenic Complex Hyperkinetic Disorders.

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P2860

P2860

Emerging Monogenic Complex Hyperkinetic Disorders.

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P1476

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P2888

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