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Browsing by Author Jasinge, E.
Showing results 1 to 3 of 3
Issue Date | Title | Author(s) |
2022 | A case of multiple sulfatase deficiency | Razeen, Z.; Suriapperuma, T.; Fernando, S.; Munasinghe, R.; Jasinge, E.; Panapitiya, M. |
2020 | A Novel mutation in ACAT1 causing Beta-Ketothiolase deficiency in a 4-year-old Sri Lankan boy with metabolic ketoacidosis. | Manawadu, T. V.; Jasinge, E.; Fernando, M.; Gamage, P.; Gunarathne, A.V. |
2021 | A rare co-occurrence of duchenne muscular dystrophy, congenital adrenal hypoplasia and glycerol kinase deficiency due to Xp21 contiguous gene deletion syndrome: case report. | Rathnasiri, A.; Senarathne, U.; Arunath, V.; Hoole, T.; Kumarasiri, I.; Muthukumarana, O.; Jasinge, E.; Mettananda, S. |