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
Analysis of the developmental SIX6 homeobox gene in patients with anophthalmia/microphthalmia
✍ Scribed by M.E. Gallardo; S. Rodríguez de Córdoba; A.S. Schneider; M.A. Dwyer; C. Ayuso; P. Bovolenta
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 151 KB
- Volume
- 129A
- Category
- Article
- ISSN
- 1552-4825
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