Hereditary hepatic porphyria with delta aminolevulinate dehydrase deficiency: Immunologic characterization of the non-catalytic enzyme
Human Genetics, ISSN: 0340-6717, Vol: 69, Issue: 2, Page: 174-177
1985
- 24Citations
- 3Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations24
- Citation Indexes24
- 24
- CrossRef17
- Captures3
- Readers3
Article Description
Immunoreactive δ-aminolevulinate dehydrase (ALA-D) was measured in lysates from two porphyric patients with ALA-D deficiency (enzyme activities were below 2% of the normal level). By using two different immunologic methods, we found a cross-reactive immunologic material (CRIM+) which corresponded to 20% and 33% of the control level. Therefore the molecular basis that accounts for the deficiency of ALA-D in these patients is a structurally modified enzyme. The methods used to determine the molecular weight (by Western blotting) and the isoelectric point (by chromatofocusing) of the mutants did not show any difference by comparison with the normal enzyme. © 1985 Springer-Verlag.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0021991595&origin=inward; http://dx.doi.org/10.1007/bf00293292; http://www.ncbi.nlm.nih.gov/pubmed/3882553; http://link.springer.com/10.1007/BF00293292; http://link.springer.com/content/pdf/10.1007/BF00293292; https://dx.doi.org/10.1007/bf00293292; https://link.springer.com/article/10.1007/BF00293292
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