This study offers important insight into the pathogenic basis of intragenic frameshift deletions in the carboxy-terminal domain of MECP2, which account for some Rett syndrome cases, yet similar ...
Modern Engineering Marvels on MSN
GRIN2A null variants linked to childhood-onset mental disorders and L-serine therapy
Could one genetic mutation be sufficient to bring on complex psychopathology? For decades, dominant models of mental ...
Morning Overview on MSN
This rare mutation destroys brain cells, scientists found the cause
Scientists have traced a devastating pattern of brain cell loss in a handful of families to a single, ultra-rare mutation ...
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