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The Screening of Hereditary Metabolic Defects Among Newborn Infants
The present communciation describes the use of four approaches to the detection of hereditary metabolic disorders: (1) the bacterial inhibition assay, (2) the reduction of nicotinamide adenine dinucleotide phosphate (NADP), (3) the use of paper chromatography, and (4) other specific methods. Using s...
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| Autor principal: | |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
1966
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1935513/ https://ncbi.nlm.nih.gov/pubmed/4380501 |
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