Rett-like Phenotypes in HNRNPH2-Related Neurodevelopmental Disorder
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DOI: 10.3390/genes14061154
Abstract: Rett Syndrome (RTT) is a neurodevelopmental disorder with a prevalence of 1:10,000 to 15,000 females worldwide. Classic Rett Syndrome presents in early childhood with a period of developmental regression, loss of purposeful hand skills along… read more here.
Keywords: neurodevelopmental disorder; atypical rtt; related neurodevelopmental; hnrnph2 related ... See more keywords