The causative gene behind rare genetic disorder, which delays development of motor activities in children has been discovered by scientists. The study was done on a four-year-old child from Punjab, and nine other children who were suffering from motor developmental delay. They could not walk and sit without support. The team, led by Ryan Taft of the University of Queensland's Institute for Molecular Bioscience (IMB), comprised 16 researchers including ...
via Medindia Health News
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