Vivienne C. M. Neeve

A new phenotype of brain iron accumulation with dystonia, optic atrophy, and peripheral neuropathy

B. Keavney, M. Santibanez-Koref, P. Chinnery, 2012, Movement disorders : official journal of the Movement Disorder Society.

Clinical and functional characterisation of the combined respiratory chain defect in two sisters due to autosomal recessive mutations in MTFMT

P. Bauer, M. Santibanez-Koref, P. Chinnery, 2013, Mitochondrion.

Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies.

Beril Talim, Patrick F Chinnery, Robert W Taylor, 2014, JAMA.

Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency

Robert W. Taylor, J. Kemp, P. Chinnery, 2010, Brain : a journal of neurology.

What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr?

Robert W. Taylor, S. Dimauro, H. Smeets, 2012, Brain : a journal of neurology.