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. 1990 Oct 11;18(19):5915–5916. doi: 10.1093/nar/18.19.5915

Identification of a common nonsense mutation in Japanese patients with type I adenine phosphoribosyltransferase deficiency.

A Sahota ¹, J Chen ¹, K Asaki ¹, H Takeuchi ¹, P J Stambrook ¹, J A Tischfield ¹

PMCID: PMC332361 PMID: 1977137

Selected References

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

Hidaka Y., Palella T. D., O'Toole T. E., Tarlé S. A., Kelley W. N. Human adenine phosphoribosyltransferase. Identification of allelic mutations at the nucleotide level as a cause of complete deficiency of the enzyme. J Clin Invest. 1987 Nov;80(5):1409–1415. doi: 10.1172/JCI113219. [DOI] [PMC free article] [PubMed] [Google Scholar]
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