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Article

Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosis

16 Mar 2012

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Share to Amyotrophic Lateral Sclerosis Research
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 22425014
DOI: 10.1016/j.jns.2012.02.029

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Related research

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Research trail→

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Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosisPMID 22425014Read ↗

H63D CG genotype of HFE is associated with increased risk of sporadic amyotrophic lateral sclerosis in a single population.Semantic proximity Read ↗

Mutations in the HFE gene and sporadic amyotrophic lateral sclerosis risk: a meta-analysis of observational studies.Semantic proximity Read ↗

The association between H63D mutations in HFE and amyotrophic lateral sclerosis in a Dutch population.Semantic proximity Read ↗

Repeat expansion in C9ORF72 is not a major cause of amyotrophic lateral sclerosis among Iranian patientsSemantic proximity Read ↗

Frequency of C9orf72 repeat expansions in amyotrophic lateral sclerosis: a Belgian cohort studySemantic proximity Read ↗

H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis.Semantic proximity Read ↗

Genotype-phenotype correlation in Tunisian patients with Amyotrophic Lateral SclerosisSemantic proximity Read ↗

H63D polymorphism in the hemochromatosis gene is associated with sporadic amyotrophic lateral sclerosis in China.Semantic proximity Read ↗

A new polymorphism in the human HFE gene.Semantic proximity Read ↗

HFE H63D polymorphism is increased in patients with amyotrophic lateral sclerosis of Italian originSemantic proximity Read ↗

Intragenic haplotype analysis of common HFE mutations in the Portuguese population.Semantic proximity Read ↗

Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patients.Semantic proximity Read ↗

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