Sodium Channel Myotonia and a Novel Gly701Asp Mutation in the SCN4A Gene: From an Ophthalmological Symptom to a Familial Disease

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Source: Neuro-Ophthalmology - July 23, 2020 Category: Opthalmology Authors: Filipa Sampaio S érgia Soares Sara Pereira Jos é Alberto Lemos Ágata Mota Source Type: research