Items where authors include "Kurian, M.A."

Article

Vezyroglou, A., Akilapa, R., Barwick, K. et al. (26 more authors) (2022) The phenotypic continuum of ATPLA3-related disorders. Neurology, 99 (14). ISSN 0028-3878

Nolden, K.A., Egner, J.M., Collier, J.J. et al. (21 more authors) (2022) Novel DNM1L variants impair mitochondrial dynamics through divergent mechanisms. Life Science Alliance, 5 (12). ARTN e202101284.

Ito, Y., Carss, K.J., Duarte, S.T. et al. (18 more authors) (2018) De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures. The American Journal of Human Genetics, 103 (1). pp. 144-153. ISSN 0002-9297

Sadleir, L.G., Mountier, E.I., Gill, D. et al. (13 more authors) (2017) Not all SCN1A epileptic encephalopathies are Dravet syndrome. Neurology, 89 (10). pp. 1035-1042. ISSN 0028-3878