Team led by institute for basic research scientist publishes findings on TAF1 syndrome

(NYS Institute for Basic Research in Developmental Disabilities) An international research team led by Dr. Gholson Lyon of the New York State Office for People With Developmental Disabilities' Institute for Basic Research in Developmental Disabilities announced publication in Human Mutation of findings from its study of the rare disease TAF1 syndrome. The team previously identified the syndrome, caused by pathogenic variants involving the X-linked gene TAF1, in 11 families. In this recent study, the researchers identified an additional 27 families with the syndrome.
Source: EurekAlert! - Biology - Category: Biology Source Type: news