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http://hub.abes.fr/bmj/periodical/bjo/2010/volume_95/issue_6/B3544029186F2E71E053120B220AF726/authorship/4
http://hub.abes.fr/bmj/periodical/jnnp/2010/volume_81/issue_5/B35A17CA1BD55B19E053120B220AE1F6/authorship/8
http://hub.abes.fr/bmj/periodical/jmedgenet/2004/volume_41/issue_9/B3598D6B61DF7CBEE053120B220A90C5/authorship/1
http://hub.abes.fr/oup/periodical/jid/1993/volume_168/issue_5/101093infdis16851328/authorship/5
http://hub.abes.fr/oup/periodical/brainj/2008/volume_131/issue_2/101093brainawm272/authorship/10
http://hub.abes.fr/oup/periodical/molehr/1997/volume_3/issue_9/101093molehr39811/authorship/2
http://hub.abes.fr/bmj/periodical/jmg/2013/volume_50/issue_10/B35958AFB11D6AAFE053120B220A26C8/authorship/24
http://hub.abes.fr/oup/periodical/brainj/2008/volume_131/issue_2/101093brainawm298/authorship/3
http://hub.abes.fr/oup/periodical/humrep/2005/volume_20/issue_3/101093humrepdeh667/authorship/6
http://hub.abes.fr/oup/periodical/molehr/2001/volume_7/issue_5/101093molehr75425/authorship/1
http://hub.abes.fr/oup/periodical/brainj/2010/volume_133/issue_3/101093brainawq007/authorship/23
http://hub.abes.fr/oup/periodical/humrep/2003/volume_18/issue_3/101093humrepdeg096/authorship/7
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OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus’ phenotypes
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance
Mitochondrial DNA content affects the fertilizability of human oocytes
Oligoasthenospermia associated with multiple mitochondrial DNA rearrangements.
Low oocyte mitochondrial DNA content in ovarian insufficiency
Increased sperm mitochondrial DNA content in male infertility
Hepatitis C Virus Genotypes in Chronic Hepatitis and Response to Interferon-α Therapy
Multi-system neurological disease is common in patients with OPA1 mutations
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