THE several rare familial disorders constituting the "congenital methemoglobinemias" arise from either of two kinds of inborn errors of metabolism. One kind, accounting for the hemoglobin-M group, ...
Investigation of the electrophoretic characteristics of NADH methemoglobin reductase in five unrelated families with a deficiency of this enzyme showed three different types of enzyme patterns: total ...
You have full access to this article via your institution. Figure 1: EPR spectra of solutions of nitrite–methemoglobin in HEPES buffer, pH 7.4.
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback