## Abstract Ataxia telangiectasia (A‐T) is a progressive neurodegenerative disease with onset in early childhood, caused by mutations in the __ATM__ (ataxia‐telangiectasia mutated) gene. Diagnosis relies on laboratory tests showing high levels of serum alphafetoprotein, cell sensitivity to ionizing
✦ LIBER ✦
Two-tier analysis of histone H2AX phosphorylation allows the identification of Ataxia Telangiectasia heterozygotes
✍ Scribed by Paola Porcedda; Valentina Turinetto; Luca Orlando; Erica Lantelme; Alfredo Brusco; Mario De Marchi; Antonio Amoroso; Umberto Ricardi; Dario Gregori; Claudia Giachino
- Book ID
- 118497339
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- English
- Weight
- 182 KB
- Volume
- 92
- Category
- Article
- ISSN
- 0167-8140
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