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. 1977 Nov;29(6):642–644.

Adenosine deaminase deficiency: another family with "silent" ADA allele and normal ADA activity in two heterozygotes.

S H Chen, C R Scott, E R Giblett, A S Levin

PMCID: PMC1685505 PMID: 930931

644

Selected References

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

Brinkmann B., Brinkmann M., Martin H. A new allele in red cell adenosine deaminase polymorphism: ADA. Hum Hered. 1973;23(6):603–607. doi: 10.1159/000152627. [DOI] [PubMed] [Google Scholar]
Chen S. H., Scott R., Giblett E. R. Adenosine deaminase: demonstration of a "silent" gene associated with combined immunodeficiency disease. Am J Hum Genet. 1974 Jan;26(1):103–107. [PMC free article] [PubMed] [Google Scholar]
Hirschhorn R. Defects of purine metabolism in immunodeficiency diseases. Prog Clin Immunol. 1977;3:67–83. [PubMed] [Google Scholar]
Trotta P. P., Smithwick E. M., Balis M. E. A normal level of adenosine deaminase activity in the red cell lysates of carriers and patients with severe combined immunodeficiency disease. Proc Natl Acad Sci U S A. 1976 Jan;73(1):104–108. doi: 10.1073/pnas.73.1.104. [DOI] [PMC free article] [PubMed] [Google Scholar]

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