A new culprit in Huntington’s: Brain organoid model implicates gene in disease progression

A new culprit in Huntington’s: Brain organoid model implicates gene in disease progression

For the first time, researchers have implicated the gene CHCHD2 in Huntington’s disease (HD)—an incurable genetic neurodegenerative disorder—and identified the gene as a potentially new therapeutic target. In a brain organoid model of the disease, the researchers found that mutations in the Huntington gene HTT also affect CHCHD2, which is involved in maintaining the normal function of mitochondria.

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