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 ...
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