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Article

ATXN2 CAG repeat expansions increase the risk for Chinese patients with amyotrophic lateral sclerosis

28 Apr 2013

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 23635656
DOI: 10.1016/j.neurobiolaging.2013.04.009

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ATXN2 CAG repeat expansions increase the risk for Chinese patients with amyotrophic lateral sclerosisPMID 23635656Read ↗

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Interrupted CAG expansions in ATXN2 gene expand the genetic spectrum of frontotemporal dementiasSemantic proximity Read ↗

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Intermediate CAG repeat expansion in the ATXN2 gene is a unique genetic risk factor for ALS--a systematic review and meta-analysis of observational studies.Semantic proximity Read ↗

Amyotrophic Lateral Sclerosis Risk for Spinocerebellar Ataxia Type 2 ATXN2 CAG Repeat AllelesSemantic proximity Read ↗

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ATXN-2 CAG repeat expansions are interrupted in ALS patientsSemantic proximity Read ↗

Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohortSemantic proximity Read ↗

Identification of GGC repeat expansion in the NOTCH2NLC gene in amyotrophic lateral sclerosis.Semantic proximity Read ↗

ATXN2 trinucleotide repeat length correlates with risk of ALS.Semantic proximity Read ↗

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