A. Butterworth

Clinical and molecular characteristics of mitochondrial DNA depletion syndrome associated with neonatal cholestasis and liver failure.

Robert W. Taylor, E. Faqeih, A. El-Hattab, 2014, The Journal of pediatrics.

MPV17 mutation causes neuropathy and leukoencephalopathy with multiple mtDNA deletions in muscle

Robert W. Taylor, I. Bodi, R. Hadden, 2012, Neuromuscular Disorders.

Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene

Robert W. Taylor, N. Ashley, A. Seller, 2013, European Journal of Human Genetics.