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GENE-EDITING OF FMR1 USING CRISPR/CAS9
Market NeedFragile X syndrome is an X-chromosome-linked disease that affects males more severely than females and is the most common cause of inherited intellectual disability, often co-occurring with Autism spectrum disorder. According to the CDC, around 1 in every 6000 males and 7000 females are born with the condition. Patients usually present with...
Published: 2/27/2018   |   Inventor(s): Beverly Davidson, Carolyn Yrigollen, Alejandro Mas Monteys
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Category(s): Therapeutic