Presynaptic congenital myasthenic syndrome due to three novel mutations in SLC5A7 encoding the sodium-dependant high-affinity choline transporter
publicat a: Neuromuscular Disorders
date of publication: 2020-10-20
tema principal: congenital myasthenic syndrome, presynaptic congenital myasthenic syndrome
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Article - wd:Q103722792