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Results of search for 'au:"Chatzoglou, E"'
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Authors
Amselem, S
Bataillard, M
Blondy, P
Chatzoglou, E
Eymard, B
Fardeau, M
Fayet, G
Frachon, P
Godinot, C
Jardel, C
Laforêt, P
Legros, F
Lombès, A
Maisonobe, T
Ogier De Baulny, H
Rumbach, L
Sternberg, D
Tournade, A
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Topics
Adolescent
Adult
Aged
Amino Acid Substitution
Antimycin A
Blotting, Western
Child
Child, Preschool
Cytochrome b Group
DNA Mutational Analysis
DNA, Mitochondrial
Genetic Variation
Haplotypes
Humans
Male
Middle Aged
Mitochondrial Myopathies
Point Mutation
RNA, Transfer
genetics
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English
Your search returned 3 results.
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1.
Functional characterization of novel mutations in the human cytochrome b gene.
[electronic resource]
by
Legros, F
Chatzoglou, E
Frachon, P
Ogier De Baulny, H
Laforêt, P
Jardel, C
Godinot, C
Lombès, A
Producer:
20010830
In:
European journal of human genetics : EJHG
vol. 9
Online resources:
Available from publisher's website
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2.
Atypical MELAS syndrome associated with a new mitochondrial tRNA glutamine point mutation.
[electronic resource]
by
Bataillard, M
Chatzoglou, E
Rumbach, L
Sternberg, D
Tournade, A
Laforêt, P
Jardel, C
Maisonobe, T
Lombès, A
Producer:
20010405
In:
Neurology
vol. 56
Online resources:
Available from publisher's website
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No items available.
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3.
Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders.
[electronic resource]
by
Sternberg, D
Chatzoglou, E
Laforêt, P
Fayet, G
Jardel, C
Blondy, P
Fardeau, M
Amselem, S
Eymard, B
Lombès, A
Producer:
20010531
In:
Brain : a journal of neurology
vol. 124
Online resources:
Available from publisher's website
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No items available.
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