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Showing results (181-190 of 184) with videos related to

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Nature Genetics|June 30, 2001
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondriaJ N Spelbrink, F Y Li, V Tiranti, et al.
Journal of Neurology|July 12, 2017
Revisiting mitochondrial ocular myopathies: a study from the Italian NetworkD Orsucci, C Angelini, E Bertini, et al.
Brain : a Journal of Neurology|February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutationsP Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
European Journal of Human Genetics : EJHG|October 31, 2002
Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosisC Dobson-Stone, A Danek, L Rampoldi, et al.
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Showing results (181-190 of 184) with videos related to

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Pageof 19
You have reached the last page of results.This site can display upto 184 results.
Nature Genetics|June 30, 2001
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondriaJ N Spelbrink, F Y Li, V Tiranti, et al.
Journal of Neurology|July 12, 2017
Revisiting mitochondrial ocular myopathies: a study from the Italian NetworkD Orsucci, C Angelini, E Bertini, et al.
Brain : a Journal of Neurology|February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutationsP Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
European Journal of Human Genetics : EJHG|October 31, 2002
Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosisC Dobson-Stone, A Danek, L Rampoldi, et al.
Pageof 19