A. Dalton

Clinical features of hereditary spastic paraplegia due to spastin mutation

Christopher McDermott, Christine Burness, Janine Kirby et al. · Neurology · 2006 · 136 citations

Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK.

Jayne Leggo, A. Dalton, Patrick J. Morrison et al. · Journal of Medical Genetics · 1997 · 78 citations · Full text

High frequency of missense mutations in glycogen storage disease type VI

Nicholas Beauchamp, Joanna Taybert, M. P. Champion et al. · Journal of Inherited Metabolic Disease · 2007 · 56 citations · Full text

Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency

S. E. Olpin, Amal Afifi, S. Clark et al. · Journal of Inherited Metabolic Disease · 2003 · 52 citations

Neonatal Screening for Cystic Fibrosis in the Trent Region (UK): Two-Stage Immunoreactive Trypsin Screening Compared with a Three-Stage Protocol with DNA Analysis as an Intermediate Step

R. J. Pollitt, A. Dalton, Steve O. Evans et al. · Journal of Medical Screening · 1997 · 38 citations