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Identification of a point mutation in the adenosine deaminase gene responsible for immunodeficiency.
Deficiency of adenosine deaminase (ADA) is the cause of an autosomal recessive form of immunodeficiency. We sought to define, at a molecular level, the mutations responsible for ADA deficiency in the cell line GM-1715, derived from an immunodeficient patient. Full-length complementary DNA (cDNA) for...
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| Publicado no: | J Clin Invest |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Clinical Investigation
1985
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC423929/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3839802/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI112050 |
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