Publications by authors named "Matthew J Parton"

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Differential phenotypic expression of a novel PDHA1 mutation in a female monozygotic twin pair.
Alejandro Horga, Catherine E Woodward, Alberto Mills, Isabel Pareés, Iain P Hargreaves, Matthew J Parton

Hum Genet· December 2019

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Two families with familial amyotrophic lateral sclerosis are linked to a novel locus on chromosome 16q.
Deborah M Ruddy, Matthew J Parton, Ammar Al-Chalabi, Cathryn M Lewis, Caroline Vance

Am J Hum Genet· August 2003

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Ciliary neurotrophic factor genotype does not influence clinical phenotype in amyotrophic lateral sclerosis.
Ammar Al-Chalabi, Margaret D Scheffler, Bradley N Smith, Matthew J Parton, Merit E Cudkowicz

Ann Neurol· July 2003

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D90A-SOD1 mediated amyotrophic lateral sclerosis: a single founder for all cases with evidence for a Cis-acting disease modifier in the recessive haplotype.
Matthew J Parton, Wendy Broom, Peter M Andersen, Ammar Al-Chalabi, P Nigel Leigh

Hum Mutat· December 2002

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