Molecular basis of recessive congenital methemoglobinemia, types I and II: Exon skipping and three novel missense mutations in the NADH-cytochrome b5 reductase (diaphorase 1) gene

Kugler, WilfriedWilfriedKuglerPekrun, ArnulfArnulfPekrunLaspe, PetraPetraLaspeErdlenbruch, BernhardBernhardErdlenbruchLakomek, MaxMaxLakomek2021-06-012021-06-012001https://resolver.sub.uni-goettingen.de/purl?gro-2/86754enMolecular basis of recessive congenital methemoglobinemia, types I and II: Exon skipping and three novel missense mutations in the NADH-cytochrome b5 reductase (diaphorase 1) genejournal_article10.1002/humu.31