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Characterization of the Porphobilinogen Deaminase Deficiency in Acute Intermittent Porphyria

The molecular pathology of the porphobilinogen (PBG)-deaminase deficiency in heterozygotes for acute intermittent porphyria (AIP) was investigated by means of biochemical and immunologic techniques. The stable enzyme-substrate intermediates (A, B, C, D, and E) of PBG-deaminase were separated by anio...

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Detaylı Bibliyografya
Yayımlandı:J Clin Invest
Asıl Yazarlar: Anderson, Peter M., Reddy, Raman M., Anderson, Karl E., Desnick, Robert J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Clinical Investigation 1981
Konular:
Online Erişim:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC370766/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7251856/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI110223
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