COMBINEDBrain receives grant from the Chan Zuckerberg Initiative to accelerate research for rare neurological disorders |
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The latest autism news from News Medical |
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| | A new treatment option has been discovered for fragile X syndrome, which is the most common genetic cause of autism spectrum disorders and is defined by a hereditary repetition of certain nucleotides in the DNA sequence of the FMR1 gene. Researchers at Massachusetts General Hospital (MGH) carried out the study, which was published in the journal Cell. | | | | Cold Spring Harbor Laboratory researchers have flipped the script on autism spectrum disorder (ASD) genetics. | |
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