E. Dunne

Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2

J. Schulz, C. Shaw, L. Schöls, 2004, Nature Genetics.

Hailey-Hailey disease: molecular and clinical characterization of novel mutations in the ATP2C1 gene.

A. Monaco, T. Strachan, R. Sudbrak, 2002, The Journal of investigative dermatology.

Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34.

A. Taylor, S. Huson, M. Hannan, 2000, American journal of human genetics.

Evidence for a new tumour suppressor locus (DBM) in human B–cell neoplasia telomeric to the retinoblastoma gene

F. Ross, C. M. Steel, E. Dunne, 1993, Nature Genetics.

Refined linkage disequilibrium and physical mapping of the gene locus for X-linked dystonia-parkinsonism (DYT3).

A. Monaco, R. Cox, H. Ropers, 1999, Genomics.

Do the same genes predispose to Gilles de la Tourette syndrome and dystonia? Report of a new family and review of the literature

K. Mills, A. Nemeth, J. Elston, 1999, Movement disorders : official journal of the Movement Disorder Society.