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. 1991 Apr 25;19(8):1966. doi: 10.1093/nar/19.8.1966

PCR detection of a G/T polymorphism at exon 10 of the porphobilinogen deaminase gene (PBG-D).

X F Gu ¹, J S Lee ¹, M H Delfau ¹, B Grandchamp ¹

PMCID: PMC328159 PMID: 2030987

1966

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Grandchamp B., Picat C., de Rooij F., Beaumont C., Wilson P., Deybach J. C., Nordmann Y. A point mutation G----A in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyria. Nucleic Acids Res. 1989 Aug 25;17(16):6637–6649. doi: 10.1093/nar/17.16.6637. [DOI] [PMC free article] [PubMed] [Google Scholar]

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