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Molecular analysis of porphobilinogen (PBG) deaminase gene mutations in acute intermittent porphyria: first study in patients of Slavic origin
R. Rosipal, H. Puy, J. Lamoril
Scandinavian journal of clinical & laboratory investigation.
1997 ;
Roč. 57 (č. 3) :
s. 217-224.
Language English Country Norway
Persistent link
https://www.medvik.cz/link/bmc98007244
- MeSH
- Porphyria, Acute Intermittent genetics blood urine MeSH
- Exons MeSH
- Genetic Testing MeSH
- Hydroxymethylbilane Synthase genetics blood MeSH
- Introns MeSH
- Humans MeSH
- Mutation MeSH
- Porphobilinogen urine MeSH
- Check Tag
- Humans MeSH
- Geographicals
- Czech Republic MeSH
- Slovakia MeSH
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