Spinocerebellar Ataxia 27: A Review and Characterization of an Evolving Phenotype.

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Spinocerebellar Ataxia 27: A Review and Characterization of an Evolving Phenotype.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Spinocerebellar Ataxia 27: A Review and Characterization of an Evolving Phenotype.

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Spinocerebellar Ataxia 27: A Review and Characterization of an Evolving Phenotype.

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Spinocerebellar Ataxia 27: A Review and Characterization of an Evolving Phenotype.

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Spinocerebellar Ataxia 27: A Review and Characterization of an Evolving Phenotype.

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Spinocerebellar Ataxia 27: A Review and Characterization of an Evolving Phenotype.

@en

Spinocerebellar Ataxia 27: A Review and Characterization of an Evolving Phenotype.

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P1476

Spinocerebellar Ataxia 27: A Review and Characterization of an Evolving Phenotype

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P2093

Brian D Berman

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Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International

P2860

Fibroblast growth factor 14 is an intracellular modulator of voltage-gated sodium channels

A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected]

Episodic Ataxias: Clinical and Genetic Features

Parkinsonism in spinocerebellar ataxia

Intracellular Fibroblast Growth Factor 14: Emerging Risk Factor for Brain Disorders.

Ataxia and paroxysmal dyskinesia in mice lacking axonally transported FGF14.

Mutation analysis in the fibroblast growth factor 14 gene: frameshift mutation and polymorphisms in patients with inherited ataxias.

Autosomal dominant cerebellar ataxias: a systematic review of clinical features.

Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene (SCA27): A new phenotype.

Intracellular FGF14 (iFGF14) Is Required for Spontaneous and Evoked Firing in Cerebellar Purkinje Neurons and for Motor Coordination and Balance

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scholarly article

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10.7916/D80S0ZJQ

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Christopher L Groth

Brian D Berman

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ScienceSource

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2018-01-30T00:00:00Z

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29416937

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P921

Marinesco-Sjogren syndrome

spinocerebellar degenerations

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5801325

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