A Silent Gene Speaks: The Molecular Etiology of a Rare Neurological Disorder Finally Explained
被遗忘的基因:揭开一种罕见神经疾病的分子病因
A study published in *Nature Neuroscience* identifies a previously overlooked recessive gene mutation that disrupts the endoplasmic reticulum–mitochondria axis, providing the long-sought molecular cause of a rare neurodegenerative disorder.