Family Phenotypic Heterogeneity Caused by Mitochondrial DNA Mutation A3243G
Maternally inherited diabetes and deafness is a rare form of diabetes caused by a mitochondrial DNA mutation. The index case is a 55-year-old woman who was admitted with hypertrophic cardiomyopathy. She had a history of diabetes mellitus and hearing loss. The patient’s mother, two brothers and two s...
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| Outros Autores: | , , |
| Formato: | article |
| Idioma: | eng |
| Publicado em: |
2017
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| Texto completo: | https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/8638 |
| País: | Portugal |
| Oai: | oai:ojs.www.actamedicaportuguesa.com:article/8638 |