Human Xp22.2 has been proposed as a candidate region for the Rett syndrome (RTT) gene. M6b, a member of the proteolipid protein gene family, was mapped to Xp22.2 within one of the RTT candidate regions. In this article we describe the structure of the M6b gene, refine the physical mapping of M6b bet
✦ LIBER ✦
Mutation analysis of the MECP2 gene in patients with Rett syndrome
✍ Scribed by Francesca L. Conforti; Rosalucia Mazzei; Angela Magariello; Alessandra Patitucci; Anna L. Gabriele; Maria Muglia; Aldo Quattrone; Agata Fiumara; Rita Barone; Lorenzo Pavone; Rita Nisticò; Loredana Mangone
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 46 KB
- Volume
- 117A
- Category
- Article
- ISSN
- 1552-4825
No coin nor oath required. For personal study only.
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