Case report: Novel compound heterozygosity for pathogenic variants in MED23 in a syndromic patient with postnatal microcephaly

Case report: Novel compound heterozygosity for pathogenic variants in MED23 in a syndromic patient with postnatal microcephaly https://t.co/xrpfcWXs4Q https://t.co/d88Uafkl5H

New Research: Case report: Novel compound heterozygosity for pathogenic variants in MED23 in a syndromic patient with postnatal microcephaly: Biallelic loss-of-function variants in MED23 cause a recessive syndromic intellectual disability… https://t.co/BiJ