Garry K. Brown

SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome

Zhiqing Zhu, Jianbo Yao, Timothy Johns et al. · Nature Genetics · 1998 · 625 citations

Life Sciences, Genetics, Molecular Biology +5

Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5

Peter R. Baker, Marisa W. Friederich, Michael A. Swanson et al. · Brain · 2013 · 223 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Families of mtDNA re-arrangements can be detected in patients with mtDNA deletions: duplications may be a transient intermediate form

Joanna Poulton, Mary E. Deadman, Karl Morten et al. · Human Molecular Genetics · 1993 · 161 citations

Medicine, Genetics, Molecular Genetics +14

A new point mutation associated with mitochondrial encephalomyopathy

Karl Morten, Jonathan M. Cooper, Garry K. Brown et al. · Human Molecular Genetics · 1993 · 139 citations

Life Sciences, Genetics, Molecular Genetics +17

X-Chromosome localization of the functional gene for the E1α subunit of the human pyruvate dehydrogenase complex

Ruth M. Brown, Hans‐Henrik M. Dahl, Garry K. Brown · Genomics · 1989 · 136 citations

Life Sciences, Genetics, Molecular Biology +10