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Rethinking the fate of males with mutations in the gene that causes Rett syndrome

โœ Scribed by Carolyn Schanen


Book ID
117545553
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
54 KB
Volume
23
Category
Article
ISSN
0387-7604

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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