The 2018 version of the gene table of monogenic neuromuscular disorders (nuclear genome)
Mots clés
Congenital myasthenic syndromes
Motor neurone diseases
Other myopathies
Hereditary motor and sensory neuropathies
Hereditary ataxias
Ion channel muscle diseases
Myotonic syndromes
Malignant hyperthermias
Congenital myopathies
Distal myopathies
Hereditary cardiomyopathies
Metabolic myopathies
Congenital muscular dystrophies
Muscular dystrophies
Hereditary paraplegias
Other neuromuscular disorders
Origine | Fichiers produits par l'(les) auteur(s) |
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