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A new mutation in the FUS gene, which results in a shorter version of the FUS protein that cannot enter form the cell nucleus to work as it

Research conducted at The Ohio State University Wexner Medical Center and The Ohio State University College of Medicine found that SCI in...

Mutations in the MECP2 gene, which lead to most cases of Rett syndrome, prevent the formation of droplet-like structures that regulate DNA.

A new report, released yesterday by the Australian Institute for Health and Welfare (AIHW) confirms how widespread mental illness...

Duchenne muscular dystrophy (DMD) is a rapidly progressive form of muscular dystrophy caused by a mutation in the DMD gene.

Dr Dinesh Palipana had struggled to maintain employment that was otherwise guaranteed to medical graduates because of a spinal cord injury.

Levels of inflammatory markers in the lungs may help predict pulmonary exacerbations in children with cystic fibrosis (CF).

New discoveries about the disruption of condensates in the neurodevelopmental disorder Rett syndrome provide insights into how cells compar