## Abstract Rett syndrome (RTT) is an X‐linked dominant neurodevelopmental disorder affecting almost exclusively girls. Although mutations in methyl‐CpG‐binding protein (MeCP2) are known to be associated with RTT, gene expression patterns are not significantly altered in MeCP2‐deficient cells. A re
✦ LIBER ✦
Molecular computing as a link between biological and physical theory
✍ Scribed by Michael Conrad; E.A. Liberman
- Publisher
- Elsevier Science
- Year
- 1982
- Tongue
- English
- Weight
- 962 KB
- Volume
- 98
- Category
- Article
- ISSN
- 0022-5193
No coin nor oath required. For personal study only.
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