Interrupted CAG expansions in ATXN2 gene expand the genetic spectrum of frontotemporal dementias.

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Interrupted CAG expansions in ATXN2 gene expand the genetic spectrum of frontotemporal dementias.

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2018 nî lūn-bûn

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Interrupted CAG expansions in ...... m of frontotemporal dementias.

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Interrupted CAG expansions in ...... m of frontotemporal dementias.

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Interrupted CAG expansions in ...... m of frontotemporal dementias.

@en

Interrupted CAG expansions in ...... m of frontotemporal dementias.

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Interrupted CAG expansions in ...... m of frontotemporal dementias.

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Interrupted CAG expansions in ...... m of frontotemporal dementias.

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P1476

Interrupted CAG expansions in ...... m of frontotemporal dementias.

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P2093

Agnès Camuzat

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Charles Duyckaerts

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Clémence Fournier

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Daisy Rinaldi

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Danielle Seilhean

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Isabelle Le Ber

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Laura Molina-Porcel

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Mathieu Barbier

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Morwena Latouche

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Neuro-CEB Neuropathology Network

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P2860

Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS

A harmonized classification system for FTLD-TDP pathology

PolyQ repeat expansions in ATXN2 associated with ALS are CAA interrupted repeats

Distinct TDP-43 pathology in ALS patients with ataxin 2 intermediate-length polyQ expansions.

Criteria for the diagnosis of corticobasal degeneration

Amyotrophic lateral sclerosis risk for spinocerebellar ataxia type 2 ATXN2 CAG repeat alleles: a meta-analysis.

Spinocerebellar ataxia type 2 is associated with Parkinsonism and Lewy body pathology.

Importance of low-range CAG expansion and CAA interruption in SCA2 Parkinsonism.

Spinocerebellar ataxia type 2 (SCA2) is associated with TDP-43 pathology.

Cerebellar neuronal loss in amyotrophic lateral sclerosis cases with ATXN2 intermediate repeat expansions.

P2888

s40478-018-0547-8

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scholarly article

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10.1186/S40478-018-0547-8

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P433

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P478

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P50

Giovanni Stevanin

Vincent Anquetil

A Brice

P577

2018-05-30T00:00:00Z

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P6179

1104295915

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29848387

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5977499

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