J. Shaw

Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia.

E. Storey, I. Biros, G. Nicholson, 2000, American journal of medical genetics.

Spinocerebellar ataxia type 14: study of a family with an exon 5 mutation in the PRKCG gene

P. Lockhart, E. Storey, M. Delatycki, 2005, Journal of Neurology, Neurosurgery & Psychiatry.

Dentatorubral‐pallidoluysian atrophy in three generations, with clinical courses from nearly asymptomatic elderly to severe juvenile, in an Australian family of Macedonian descent

E. Storey, P. Mitchell, M. Fahey, 2005, American journal of medical genetics. Part A.

Spinocerebellar ataxia type 2: clinical features of a pedigree displaying prominent frontal-executive dysfunction.

E. Storey, S. Forrest, P. Mitchell, 1999, Archives of neurology.

Maternal uniparental disomy of chromosome 13 in a phenotypically normal child.

A. Bankier, S. Forrest, H. Slater, 1994, Journal of medical genetics.

Spinocerebellar ataxia type 2: clinical features of a pedigree displaying prominent frontal-executive dysfunction.

E. Storey, S. Forrest, P. Mitchell, 1999, Archives of neurology.