Whole Exome Sequencing Identifies RAI1 Mutation in a Morbidly Obese Child Diagnosed With ROHHAD Syndrome

Following our Whole Exome paper published last yr on #Genes http://t.co/14bXe7I8QF, now #JCEM publishes a similar one http://t.co/xKPca4TwcC

Whole Exome Sequencing Identifies RAI1 Mutation in a Morbidly Obese Child Diagnosed with ROHHAD Syndrome. http://t.co/w27JseCBQ1

Whole Exome Sequencing Identifies RAI1 Mutation in a Morbidly Obese Child Diagnosed with ROHHAD Syndrome. http://t.co/w27JseCBQ1