Dr Andrew Schaefer Kate Craig Sila Hopton Gavin Falkous Professor Robert Taylor et al. | Changing faces of mitochondrial disease: autosomal recessive POLG disease mimicking myasthenia gravis and progressive supranuclear palsy | 2022 |
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Kate Craig Anna Butterworth Dr Langping He Professor Robert Taylor
| Clinical and Molecular Characteristics of Mitochondrial DNA Depletion Syndrome Associated with Neonatal Cholestasis and Liver Failure | 2014 |
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Anna Butterworth Kate Craig Professor Robert Taylor
| Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene | 2014 |
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Dr Charlotte Alston Dr Andrew Schaefer Kim Krishnan Dr Langping He Kate Craig et al. | Late-Onset Respiratory Failure Due to Tk2 Mutations Causing Multiple MtDNA Deletions | 2013 |
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Dr John Yarham Dr Charlotte Alston Kate Craig Dr Kirstie Anderson Emeritus Professor Doug Turnbull et al. | Pathogenic Mitochondrial tRNA Point Mutations: Nine Novel Mutations Affirm Their Importance as a Cause of Mitochondrial Disease | 2013 |
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Dr Charlotte Alston Dr Langping He Kate Craig Dr Andrew Schaefer Professor Bobby McFarland et al. | Adults with RRM2B-related mitochondrial disease have distinct clinical and molecular characteristics | 2012 |
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Kate Craig Sharon Foster Dr Ann Curtis Professor Patrick Chinnery
| Molecular Epidemiology of Spinocerebellar Ataxia Type 6 | 2004 |
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