J. Habgood

Clinical characteristics of SOD1 gene mutations in UK families with ALS

R. Orrell, A. Malaspina, J. Habgood, 1999, Journal of the Neurological Sciences.

A new familial amyotrophic lateral sclerosis locus on chromosome 16q12.1-16q12.2.

John Mitchell, J. De Belleroche, R. Orrell, 2003, American journal of human genetics.

Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase

C. Shaw, C. Vance, M. Falchi, 2010, Proceedings of the National Academy of Sciences.

Difficulties in distinguishing sporadic from familial amyotrophic lateral sclerosis

J. Habgood, R. Lane, J. de Belleroche, 1996, Annals of neurology.

The relationship of spinal muscular atrophy to motor neuron disease: Investigation of SMN and NAIP gene deletions in sporadic and familial ALS

Richard W. Orrell, J. Belleroche, R. Orrell, 1997, Journal of the Neurological Sciences.