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Your search keyword '"Lochmüller H"' showing total 3 results

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3 results on '"Lochmüller H"'

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1. Congenital myasthenic syndrome due to DOK7 mutation in a cohort of patients with 'unexplained' limb-girdle muscular weakness.

2. Clinical variability of early-onset congenital myasthenic syndrome due to biallelic RAPSN mutations in Brazil.

3. Molecular characterisation of congenital myasthenic syndromes in Southern Brazil.

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