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Hudson G

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Publications:

Title Authors Year Journal
Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and children. Hudson G 2009 Journal of medical genetics
POLG1 mutations manifesting as autosomal recessive axonal Charcot-Marie-Tooth disease. Hudson G 2008 Archives of neurology
Reversible valproate hepatotoxicity due to mutations in mitochondrial DNA polymerase gamma (POLG1). Hudson G 2008 Archives of disease in childhood
Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and Parkinsonism. Hudson G 2007 Archives of neurology
POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions. Hudson G 2006 Neurology
Mitochondrial DNA polymerase-gamma and human disease. Hudson G 2006 Hum Mol Genet
Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene. Hudson G 2006 Brain : a journal of neurology
POLG1 in idiopathic Parkinson disease. Hudson G 2006 Neurology
Mutant POLG2 disrupts DNA polymerase gamma subunits and causes progressive external ophthalmoplegia. Hudson G 2006 Am J Hum Genet

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