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Kinetic properties of mutant deoxyguanosine kinase in a case of reversible hepatic mtDNA depletion.
Biochem J. 2007 Mar 1;402(2):377-85. doi: 10.1042/BJ20060705.
Biochem J. 2007.
PMID: 17073823
Free PMC article.
POLG exon 22 skipping induced by different mechanisms in two unrelated cases of Alpers syndrome.
Mousson de Camaret B, Chassagne M, Mayençon M, Padet S, Crehalet H, Clerc-Renaud P, Rouvet I, Zabot MT, Rivier F, Sarda P, des Portes V, Bozon D.
Mousson de Camaret B, et al. Among authors: padet s.
Mitochondrion. 2011 Jan;11(1):223-7. doi: 10.1016/j.mito.2010.07.011. Epub 2010 Aug 4.
Mitochondrion. 2011.
PMID: 20691285
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Complete loss of expression of the ANT1 gene causing cardiomyopathy and myopathy.
Echaniz-Laguna A, Chassagne M, Ceresuela J, Rouvet I, Padet S, Acquaviva C, Nataf S, Vinzio S, Bozon D, Mousson de Camaret B.
Echaniz-Laguna A, et al. Among authors: padet s.
J Med Genet. 2012 Feb;49(2):146-50. doi: 10.1136/jmedgenet-2011-100504. Epub 2011 Dec 20.
J Med Genet. 2012.
PMID: 22187496
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SURF1 deficiency causes demyelinating Charcot-Marie-Tooth disease.
Echaniz-Laguna A, Ghezzi D, Chassagne M, Mayençon M, Padet S, Melchionda L, Rouvet I, Lannes B, Bozon D, Latour P, Zeviani M, Mousson de Camaret B.
Echaniz-Laguna A, et al. Among authors: padet s.
Neurology. 2013 Oct 22;81(17):1523-30. doi: 10.1212/WNL.0b013e3182a4a518. Epub 2013 Sep 11.
Neurology. 2013.
PMID: 24027061
Free PMC article.
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