Response to the paper titled “Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy”

por Graves, Tracey D
Publicado 2018

Correction to: Episodic Ataxia Type 1: Natural History and Effect on Quality of Life

por Graves, Tracey D., Griggs, Robert C., Bundy, Brian N., Jen, Joanna C., Baloh, Robert W., Hanna, Michael G.
Publicado 2022

Episodic Ataxia Type 1: Natural History and Effect on Quality of Life

por Graves, Tracey D., Griggs, Robert C., Bundy, Brian N., Jen, Joanna C., Baloh, Robert W., Hanna, Michael G.
Publicado 2022

Mosaicism for a pathogenic MFN2 mutation causes minimal clinical features of CMT2A in the parent of a severely affected child

por Schon, Katherine, Spasic-Boskovic, Olivera, Brugger, Kim, Graves, Tracey D., Abbs, Stephen, Park, Soo-Mi, Ambegaonkar, Gautam, Armstrong, Ruth
Publicado 2017

Research priorities for mitochondrial disorders: Current landscape and patient and professional views

por Thomas, Rhys H., Hunter, Amy, Butterworth, Lyndsey, Feeney, Catherine, Graves, Tracey D., Holmes, Sarah, Hossain, Pushpa, Lowndes, Jo, Sharpe, Jenny, Upadhyaya, Sheela, Varhaug, Kristin N., Votruba, Marcela, Wheeler, Russell, Staley, Kristina, Rahman, Shamima
Publicado 2022