Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy and deafness (DIDMOAD, Wolfram syndrome).
Rötig, A
Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy and deafness (DIDMOAD, Wolfram syndrome). [electronic resource] - Journal of inherited metabolic disease 1993 - 527-30 p. digital
Publication Type: Case Reports; Journal Article
0141-8955
10.1007/BF00711672 doi
Base Sequence
Blotting, Southern
DNA Probes
DNA, Mitochondrial--genetics
Female
Humans
Infant
Lactates--metabolism
Mitochondria, Muscle--genetics
Molecular Sequence Data
Polymerase Chain Reaction
Pyruvates--metabolism
Sequence Deletion
Wolfram Syndrome--genetics
Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy and deafness (DIDMOAD, Wolfram syndrome). [electronic resource] - Journal of inherited metabolic disease 1993 - 527-30 p. digital
Publication Type: Case Reports; Journal Article
0141-8955
10.1007/BF00711672 doi
Base Sequence
Blotting, Southern
DNA Probes
DNA, Mitochondrial--genetics
Female
Humans
Infant
Lactates--metabolism
Mitochondria, Muscle--genetics
Molecular Sequence Data
Polymerase Chain Reaction
Pyruvates--metabolism
Sequence Deletion
Wolfram Syndrome--genetics