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Identification of a large-scale mitochondrial deoxyribonucleic acid deletion in endocrinopathies and deafness: report of two unrelated cases with diabetes mellitus and adrenal insufficiency, respectively.
J Clin Endocrinol Metab. 1997 Sep;82(9):3063-7. doi: 10.1210/jcem.82.9.4220.
J Clin Endocrinol Metab. 1997.
PMID: 9284744
A novel gly290asp mitochondrial cytochrome b mutation linked to a complex III deficiency in progressive exercise intolerance.
Dumoulin R, Sagnol I, Ferlin T, Bozon D, Stepien G, Mousson B.
Dumoulin R, et al. Among authors: ferlin t.
Mol Cell Probes. 1996 Oct;10(5):389-91. doi: 10.1006/mcpr.1996.0053.
Mol Cell Probes. 1996.
PMID: 8910895
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Detection of mitochondrial DNA deletions by a screening procedure using the polymerase chain reaction.
Ferlin T, Guironnet G, Barnoux MC, Dumoulin R, Stepien G, Mousson B.
Ferlin T, et al.
Mol Cell Biochem. 1997 Sep;174(1-2):221-5.
Mol Cell Biochem. 1997.
PMID: 9309691
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Segregation of the G8993 mutant mitochondrial DNA through generations and embryonic tissues in a family at risk of Leigh syndrome.
Ferlin T, Landrieu P, Rambaud C, Fernandez H, Dumoulin R, Rustin P, Mousson B.
Ferlin T, et al.
J Pediatr. 1997 Sep;131(3):447-9. doi: 10.1016/s0022-3476(97)80074-1.
J Pediatr. 1997.
PMID: 9329425
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