A new study identifies MGRN1 as linked to recessive heart and laterality defects, marking the first genotype-phenotype report in humans. This discovery enhances understanding of the genetic basis for these conditions.
mgrn1 is linked to recessive heart and laterality defects the first genotype phenotype report in humans
Original title: “MGRN1 is linked to recessive heart and laterality defects: the first genotype-phenotype report in humans.”