Hypothyroid myopathy and its association with <i>MICU1</i> gene mutations: a clinical caseauthors
Thyroid hormones are involved in the activation of glycogenolysis and mitochondrial oxidative phosphorylation. Kocher–Debré–Semelaigne Syndrome, also known as hypothyroid myopathy, is characterized by reduced glycogenolytic activity, leading to glycogen deposition in muscles. These reserves begin to...
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| Principais autores: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Endocrinology Research Centre
2025-12-01
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| coleção: | Ожирение и метаболизм |
| Assuntos: | |
| Acesso em linha: | https://www.omet-endojournals.ru/jour/article/view/13287 |
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