Acute intermittent porphyria: characterization of a novel mutation in the structural gene for porphobilinogen deaminase. Demonstration of noncatalytic enzyme intermediates stabilized by bound substrate.

To investigate the molecular pathology in acute intermittent porphyria (AIP), the nature of the defective porphobilinogen (PBG)-deaminase was determined in erythrocyte lysates from 165 AIP heterozygotes from 92 unrelated families representing 20 different ethnic or demographic groups. Immunologic an...

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Detalhes bibliográficos
Publicado no:J Clin Invest
Main Authors: Desnick, R J, Ostasiewicz, L T, Tishler, P A, Mustajoki, P
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 1985
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC423920/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3897290/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI112044
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