Title | Creator | Date | ||
---|---|---|---|---|
1 | Congenital Myasthenic Syndrome Due to Homozygous CHRNE Mutations- Report of Patients in Arabia | Salih, 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 Literature | Heidary, Gena; Calderwood, Laurel; Cox, Gerald F; Robson, Caroline D; Teot, Lisa A; Mullon, Jennifer; Anselm, Irina |