Clinical and Functional Characterization of a Missense ELF2 Variant in a CANVAS Family.

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Clinical and Functional Characterization of a Missense ELF2 Variant in a CANVAS Family.

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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

@zh-my

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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Clinical and Functional Characterization of a Missense ELF2 Variant in a CANVAS Family.

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Clinical and Functional Characterization of a Missense ELF2 Variant in a CANVAS Family.

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Item

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Clinical and Functional Characterization of a Missense ELF2 Variant in a CANVAS Family.

@en

Clinical and Functional Characterization of a Missense ELF2 Variant in a CANVAS Family.

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Clinical and Functional Characterization of a Missense ELF2 Variant in a CANVAS Family.

@en

Clinical and Functional Characterization of a Missense ELF2 Variant in a CANVAS Family.

@nl

P1476

Clinical and Functional Characterization of a Missense ELF2 Variant in a CANVAS Family

@en

P2093

Adolfo M Bronstein

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Hena Ahmad

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Marien Cobo

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P2860

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Cargo recognition failure is responsible for inefficient autophagy in Huntington's disease.

Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35).

Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia.

ETS1 regulates the expression of ATXN2.

P304

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P31

scholarly article

P356

10.3389/FGENE.2018.00085

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P478

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P50

Jose A Lopez-Escamez

Francisco Martín

Teresa Requena

Alvaro Gallego-Martinez

Lidia Frejo

P577

2018-03-23T00:00:00Z

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P698

29628936

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P932

5876245

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