Mitochondrial abnormalities in the DIDMOAD syndrome
- 1 May 1992
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 15 (3), 315-319
- https://doi.org/10.1007/bf02435965
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
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- Thiamine-responsive anemia in DIDMOAD syndromeThe Journal of Pediatrics, 1989
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- Analysis of muscle mitochondrial function with techniques applicable to needle biopsy samplesClinical Physiology and Functional Imaging, 1981
- Simultaneous Occurrence of Diabetes Mellitus, Diabetes Insipidus, and Optic Atrophy in a Brother and SisterArchives of Pediatrics & Adolescent Medicine, 1977
- Diabetes mellitus, diabetes insipidus, and optic atrophy. An autosomal recessive syndrome?Journal of Medical Genetics, 1977
- JUVENILE DIABETES MELLITUS, OPTIC ATROPHY, HEARING LOSS, DIABETES INSIPIDUS, ATONIA OF THE URINARY TRACT AND BLADDER, AND OTHER ABNORMALITIES (WOLFRAM SYNDROME)Acta Paediatrica, 1977