Rett Syndrome

RSRF-funded research reveals novel function for Rett syndrome gene

Published in Gene Therapy Weekly, November 10th, 2005

Huda Zoghbi, of Baylor College of Medicine and the Howard Hughes Medical Institute, and Juan Young, also of Baylor, and colleagues reported in the online early edition of the Proceedings of the National Academy of Science that the Rett syndrome gene, MECP2, regulates RNA splicing. This work was funded in part by the Rett Syndrome Research Foundation (RSRF).

Rett Syndrome (RTT) is a severe neurological disorder diagnosed almost exclusively in girls. Children with RTT appear to develop normally until 6 to 18 months of age, when they enter a period of regression, losing speech and motor skills. Most develop repetitive hand movements, irregular breathing patterns,...

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Source: Gene Therapy Weekly (2005-11-10)

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