Dysregulation of cotranscriptional alternative splicing underlies CHARGE syndrome

Abstract excerpt

Significance A timely diagnosis is key for both survival and quality of life of children with CHARGE syndrome (coloboma, heart defects, atresia of choanae, retardation of growth/development, genital abnormalities, and ear anomalies). Such diagnosis is often difficult to establish, in part because many patients test negative for mutation of CHD7 , the only gene associated with this condition to date. Identifying...

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