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Fragile X syndrome often results from improperly processed genetic material – correctly cutting RNA offers a potential treatment

For many people with fragile X, the mutated gene that causes symptoms is active rather than silenced. Thom Leach/Science Photo LibraryFragile X syndrome is a genetic disorder caused by a mutation in a gene that lies at the tip of the X chromosome. It is linked to autism spectrum disorders. People with fragile X experience a range of symptoms that include cognitive impairment, developmental and speech delays and hyperactivity. They may also have some physical features such as large ears and foreh

Delhi s India Gate, Mumbai s BMC Building Go Green for Awareness: All About Fragile X Gene & Autism

According to the groups working on awareness, one in 5,000 children in India is found with a Fragile X gene, which makes it approximately 4 lakh kids. Fragile X Syndrome (FXS) is a genetic condition which is the only known single-gene cause of autism

Study identifies a new potential target for treating vascular disease

Study identifies a new potential target for treating vascular disease
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