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NNMT nicotinamide N-methyltransferase, Gene ID 4837 (11q23.2, 8 exons, EC 2.1.1.1)
The XICs, TOF MS and TOF MS/MS spectra show a high level of reproducibility over the course of three consecutive days
Abstract Glucose-6-phosphate dehydrogenase (G6PD) deficiency, one of the most common human genetic enzymopathies, is caused by over 160 different point mutations and contributes to the severity of many acute and chronic diseases associated with oxidative stress, including hemolytic anemia and bilirubin-induced neurological damage particularly in newborns
The mutational constraint spectrum quantified from variation in 141,456 humans
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Kamanna, V
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