Whole-Exome Sequencing Reveals a Missense Variant c.1612C>T (p.Arg538Cys) in the BTD Gene Leading to Neuromyelitis Optica Spectrum Disorder in Saudi Families

Added 126 days ago (21.02.2022)
Authors: Muhammad Imran Naseer; Peter Natesan Pushparaj; Angham Abdulrahman Abdulkareem; Osama Y. Muthaffar
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