Gene Expression Phenotype in Heterozygous Carriers of Ataxia Telangiectasia
The defining characteristic of recessive diseases is the absence of a phenotype in the heterozygous carriers. Nonetheless, subtle manifestations may be detectable by new methods, such as expression profiling. Ataxia telangiectasia (AT) is a typical recessive disease, and individual carriers cannot b...
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| Pubblicato in: | Am J Hum Genet |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Elsevier
2002
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC378536/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12226795/ https://ncbi.nlm.nih.govhttps://doi.org/10.1086/342974 |
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