A. E. Harding

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

Albert R. La Spada, Elizabeth Wilson, Dennis B. Lubahn et al. · Nature · 1991 · 2.8K citations

Medicine, Genetics, Molecular Genetics +14

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

Ian Holt, A. E. Harding, J A Morgan-Hughes · Nature · 1988 · 1.8K citations

Life Sciences, Genetics, Molecular Genetics +14

A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.

Ian Holt, A. E. Harding, Richard Petty et al. · PubMed · 1990 · 1K citations

Life Sciences, Genetics, Molecular Genetics +14

CLASSIFICATION OF THE HEREDITARY ATAXIAS AND PARAPLEGIAS

A. E. Harding · The Lancet · 1983 · 961 citations

Life Sciences, Neurology, Neuroscience +12

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation

Paul Riordan‐Eva, M D Sanders, G.G. Govan et al. · Brain · 1995 · 483 citations

Life Sciences, Genetics, Neurology +17