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À propos de : http://hub.abes.fr/edp/periodical/medsci/2021/volume_37/issue_2021/medsci210188s/w        

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Title
  • Les neuropathies héréditaires associées au gène SORD
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Abstract
  • Mutations in the SORD gene have recently been identified as a cause of autosomal Charcot-Marie-Tooth disease as well as the underlying defect in some cases of hereditary distal motoneuronopathies. Patients may be amenable to therapies in a near future.
article type
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  • medsci210188s
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  • © 2021 médecine/sciences - Inserm
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  • médecine/sciences - Inserm
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