✦ LIBER ✦
MECP2 mutations in Danish patients with Rett syndrome: High frequency of mutations but no consistent correlations with clinical severity or with the X chromosome inactivation pattern
✍ Scribed by Nielsen, Jytte Bieber; Henriksen, Karen Friis; Hansen, Claus; Silahtaroglu, Asli; Schwartz, Marianne; Tommerup, Niels
- Book ID
- 110025091
- Publisher
- Nature Publishing Group
- Year
- 2001
- Tongue
- English
- Weight
- 163 KB
- Volume
- 9
- Category
- Article
- ISSN
- 1018-4813
No coin nor oath required. For personal study only.