Showing results (41-50 of 261) with videos related to
Sort By:
Pageof 27
Trends in Genetics : TIG|November 14, 2000
The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?P F Chinnery, D R Thorburn, D C Samuels, et al.Neurology|April 23, 2003
Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)A Agostino, L Valletta, P F Chinnery, et al.American Journal of Human Genetics|March 26, 1999
Relaxed replication of mtDNA: A model with implications for the expression of diseaseP F Chinnery, D C SamuelsClinical Neurology and Neurosurgery|December 4, 2012
Next generation sequencing for neurological diseases: new hope or new hype?M J Keogh, P F ChinneryJournal of Neurology, Neurosurgery, and Psychiatry|August 23, 2003
MitochondriaP F Chinnery, E A SchonBrain : a Journal of Neurology|January 3, 2001
The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathyP F Chinnery, D T Brown, R M Andrews, et al.Neurology|May 10, 2006
POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletionsG Hudson, M Deschauer, R W Taylor, et al.Annals of Neurology|August 12, 2000
The epidemiology of pathogenic mitochondrial DNA mutationsP F Chinnery, M A Johnson, T M Wardell, et al.Neurology|July 26, 2000
Mitochondrial DNA haplogroups and susceptibility to AD and dementia with Lewy bodiesP F Chinnery, G A Taylor, N Howell, et al.Practical Neurology|October 25, 2013
An under-recognised cause of spastic paraparesis in middle-aged womenD Bargiela, G Eglon, R Horvath, et al.Pageof 27