Les neuropathies héréditaires associées au gène SORD
Résumé
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.
Pour citer ce document
Fernández-Eulate, Gorka ; Bruneel, Arnaud ; Stojkovic, Tanya ;
Les neuropathies héréditaires associées au gène
SORD
, Med Sci (Paris), Vol. 37, N° HS ; p. 30-31 ; DOI : 10.1051/medsci/2021188