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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Dades bibliogràfiques

Publicat a:	Am J Hum Genet
Autors principals:	Watts, Jason A., Morley, Michael, Burdick, Joshua T., Fiori, Jennifer L., Ewens, Warren J., Spielman, Richard S., Cheung, Vivian G.
Format:	Artigo
Idioma:	Inglês
Publicat:	Elsevier 2002
Matèries:	Articles
Accés en línia:	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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