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nebulin
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Nemaline myopathy type 2 (NEM2): two novel mutations in the nebulin (NEB) gene.
NEB-related core-rod myopathy with distinct clinical and pathological features.
Variants in Nebulin (NEB) Are Linked to the Development of Familial Primary Angle Closure Glaucoma i…
Bilateral foot-drop as predominant symptom in nebulin (NEB) gene related "core-rod" congenital myopa…
Mutation update: the spectra of nebulin variants and associated myopathies.
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Molecular and Genetic Studies of Congenital Myopathies
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