Researchers from the Mitochondrial Medicine Program at Children's Hospital of Philadelphia (CHOP) have better characterized a ...

Scientists have uncovered how mutations in the MeCP2 gene lead to Rett syndrome, a devastating neurological disorder. By ...

There are also surgeries, including deep brain stimulation (DBS), that may help, DiGeorge syndrome is a rare genetic condition characterized by kidney and heart defects, learning disabilities, hearing ...

Under terms of the deal, Stoke will spearhead global development of zorevunersen, while Biogen will receive exclusive rights ...

A clinical research team from the LKS Faculty of Medicine, the University of Hong Kong (HKUMed), and international genetic researchers led a global research study using multi-omics analysis and ...

Klinefelter syndrome is a genetic condition that affects only males. Here's what you should know about the causes, symptoms, and treatment options for the condition. Klinefelter syndrome is a genetic ...

On Wednesday evening, 17 states who filed a lawsuit concerning Section 504 of the Rehabilitation Act told the judge that they ...

In a global study led by Dr Brian Chung Hong-yin (left), the HKUMed research team identifies a novel gene, DDX39B, for a rare ...

1. 北京天坛医院的王拥军教授与杨锋教授携手重庆医科大学的王莎莉教授团队，成功构建了一种新型猫叫综合征动物模型。