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TitleCreatorDate
1 Congenital Myasthenic Syndrome Due to Homozygous CHRNE Mutations- Report of Patients in ArabiaSalih, Mustafa A; Oystreck, Darren T; Al-Faky, Yasser H; Kabiraj, Mohammed; Omer, Mohamed I A; Subahi, Elamin M; Beeson, David; Abu-Amero, Khaled K; Bosley, Thomas M
2 Optic Atrophy and a Leigh-Like Syndrome Due to Mutations in the C12orf65 Gene: Report of a Novel Mutation and Review of the LiteratureHeidary, Gena; Calderwood, Laurel; Cox, Gerald F; Robson, Caroline D; Teot, Lisa A; Mullon, Jennifer; Anselm, Irina
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