Associated Papers
[A case of Charcot-Marie-Tooth disease type 2 caused by homozygous MME gene mutation].
Yamashiro M et al.
Rinsho Shinkeigaku = Clinical Neurology, 2023
Variants in MME are associated with autosomal-recessive distal hereditary motor neuropathy.
Hong D et al.
Annals of Clinical and Translational Neurology, 2019
Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies.
Auer-Grumbach M et al.
American Journal of Human Genetics, 2016
Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2.
Higuchi Y et al.
Annals of Neurology, 2016
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