PMID 24626631 2014 Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability.
rs1382444181 in
METTL23 gene and
Muscle hypotonia
PMID 24501276 2014 METTL23, a transcriptional partner of GABPA, is essential for human cognition.
PMID 24626631 2014 Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability.