Résultats de la recherche

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(1 - 6 of 6)
Bilateral foot-drop as predominant symptom in nebulin (NEB) gene related "core-rod" congenital myopathy
Defects in amphiphysin 2 (BIN1) and triads in several forms of centronuclear myopathies
Muscle histopathology in nebulin-related nemaline myopathy: ultrastrastructural findings correlated to disease severity and genotype
Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy

Islandora displays