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DEGOUL F
DESGUERRE I
CHARPENTIER C
FRANCOIS D
PONSOT G
DIRY M
RUSTIN P
MARSAC C
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Authors:
MARSAC C
BENELLI C
DESGUERRE I
DIRY M
FOUQUE F
DEMEIRLEIR L
PONSOT G
SENECA S
POGGI F
SAUDUBRAY JM
ZABOT MT
FONTAN D
LISSENS W
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Authors:
DEGOUL F
FRANCOIS D
DIRY M
PONSOT G
DESGUERRE I
HERON B
MARSAC C
MOUTARD ML
Citation: F. Degoul et al., A NEAR HOMOPLASMIC T8993G MTDNA MUTATION IN A PATIENT WITH ATYPIC LEIGH-SYNDROME NOT PRESENT IN THE MOTHERS TISSUES, Journal of inherited metabolic disease, 20(1), 1997, pp. 49-53
Authors:
DEGOUL F
DIRY M
RODRIGUEZ D
ROBAIN O
FRANCOIS D
PONSOT G
MARSAC C
DESGUERRE I
Citation: F. Degoul et al., CLINICAL, BIOCHEMICAL, AND MOLECULAR ANALYSIS OF A MATERNALLY INHERITED CASE OF LEIGH-SYNDROME (MILS) ASSOCIATED WITH THE MTDNA T8993G POINT MUTATION, Journal of inherited metabolic disease, 18(6), 1995, pp. 682-688
Authors:
DEGOUL F
DIRY M
POUSERRADELL A
LLORETA J
MARSAC C
Citation: F. Degoul et al., MYO-LEUKOENCEPHALOPATHY IN TWINS - STUDY OF 3243-MYOPATHY, ENCEPHALOPATHY, LACTIC-ACIDOSIS, AND STROKE-LIKE EPISODES MITOCHONDRIAL-DNA MUTATION, Annals of neurology, 35(3), 1994, pp. 365-370