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Mutational analysis of theMECP2gene in Japanese patients with Rett syndrome

✍ Scribed by K. Amano; Y. Nomura; M. Segawa; K. Yamakawa


Publisher
Nature Publishing Group
Year
2000
Tongue
English
Weight
167 KB
Volume
45
Category
Article
ISSN
1435-232X

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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