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Molecular epidemiological study of familial amyotrophic lateral sclerosis in Japanese population by whole-exome sequencing and identification of novel HNRNPA1 mutation

Amyotrophic Lateral SclerosisGenetic DisorderWhole-exome SequencingGeneticsMedicineGenetic EpidemiologyNeurologyDisease Gene IdentificationJapanese PopulationMolecular DiagnosticsNovel Hnrnpa1 Mutation