TY  - GEN
AU  - Rötig,A
AU  - Cormier,V
AU  - Chatelain,P
AU  - Francois,R
AU  - Saudubray,J M
AU  - Rustin,P
AU  - Munnich,A
TI  - Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome, MIM 222300)
SN  - 0021-9738
PY  - 1993///0413
KW  - Adolescent
KW  - Base Sequence
KW  - Blotting, Southern
KW  - DNA, Mitochondrial
KW  - genetics
KW  - Electron Transport Complex IV
KW  - metabolism
KW  - Female
KW  - Humans
KW  - Lymphocytes
KW  - enzymology
KW  - Molecular Sequence Data
KW  - Muscles
KW  - NADH Dehydrogenase
KW  - Oligodeoxyribonucleotides
KW  - Sequence Deletion
KW  - Succinate Cytochrome c Oxidoreductase
KW  - Wolfram Syndrome
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1172/JCI116267
ER  -