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Mutation analysis of 16S rRNA in patients with Rett syndrome

✍ Scribed by Judith Armstrong; Mercè Pineda; Eugènia Monrós

Book ID
117590749
Publisher
Elsevier Science
Year
2000
Tongue
English
Weight
102 KB
Volume
23
Category
Article
ISSN
0887-8994

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Mutation analysis of the M6b gene in pat
Mutation analysis of the M6b gene in patients with Rett syndrome
✍ Narayanan, Vinodh; Olinsky, Shari; Dahle, Elizabeth; Naidu, Sakkubai; Zoghbi, Hu 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 22 KB 👁 2 views

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