An Indian Case Study on Mitochondrial Neurogastrointestinal Encephalomyopathy
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is a unique autosomal recessive disorder characterized by mitochondrial changes resulting from mutations in the TYMP gene, responsible for encoding thymidine phosphorylase. Despite its genetic origin, the study indicates that the manifest...
Tallennettuna:
| Päätekijät: | , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Wolters Kluwer Medknow Publications
2024-05-01
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| Sarja: | Archives of Medicine and Health Sciences |
| Aiheet: | |
| Linkit: | https://journals.lww.com/10.4103/amhs.amhs_295_23 |
| Tagit: |
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