Diminished activity of uroporphyrinogen I-synthetase in the liver and other tissues may be regarded to be the primary genetic deficiency of acute intermittent porphyria (AIP). Increased production and renal excretion of delta-aminolevulinic acid (ALA) und porphobilinogen (PBG) are secondary phenomen
β¦ LIBER β¦
Intermittent nerve conduction
β Scribed by Chung, Shin-Ho
- Book ID
- 109703054
- Publisher
- Nature Publishing Group
- Year
- 1976
- Tongue
- English
- Weight
- 216 KB
- Volume
- 264
- Category
- Article
- ISSN
- 0028-0836
- DOI
- 10.1038/264313a0
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