Gillian Riordan

Progressive deafness–dystonia due to <i>SERAC1</i> mutations: A study of 67 cases

Roeltje R. Maas, Katarzyna Iwanicka‐Pronicka, Sema Kalkan Uçar et al. · Annals of Neurology · 2017 · 72 citations · Full text

MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load

Yi Shiau Ng, Nichola Z. Lax, Paul Maddison et al. · EBioMedicine · 2018 · 65 citations · Full text

The First Case of Riboflavin Transporter Deficiency in sub-Saharan Africa

Shaakira Chaya, Marco Zampoli, Diane Gray et al. · Seminars in Pediatric Neurology · 2017 · 24 citations

Global Health, First Case

Childhood Secondary (Symptomatic) Epilepsy, Seizure Control, and Intellectual Handicap in a Nontropical Region of South Africa

P. M. Leary, Gillian Riordan, Birgit Schlegel et al. · Epilepsia · 1999 · 21 citations · Full text

Understanding the Implications of Mitochondrial DNA Variation in the Health of Black Southern African Populations: The 2014 Workshop

Francois H. van der Westhuizen, Phumla Sinxadi, Collet Dandara et al. · Human Mutation · 2015 · 18 citations · Full text

Genetic Testing, Mtdna Variation, Genetic Epidemiology +23