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Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations
NCOA4 is a specific ferritinophagy receptor that recognize ferritin and binds to its hub subunit FTH1 and interacts with LC3, transporting ferritin to the autophagosome for lysosomal degradation and iron release (93)
Nutrients 17 (5), 794
Marcaje: se delimitan las reas donde se aplicarn las microinyecciones
Understanding these symptoms is crucial for patients taking medications that affect gastrointestinal function, as early recognition and appropriate management can prevent serious complications
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