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These findings propose the crucial role of mitochondria in ferroptosis and implicate the mitochondrial TCA cycle as a converging node for ferroptosis and cuproptosis

Disorders of GH in childhood is outlined in the Endotext chapter Disorders of Growth Hormone in Childhood by Murray and Clayton (132) Primary IGF-I deficiency or GH insensitivity is severe in homozygous genetic defects in genes including the GH receptor (Laron syndrome) gene, STAT-5b gene and IGF-I gene

2022 Mar 25;8(1):e003