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Mutation analysis of mitochondrial transfer RNA genes in rett syndrome

โœ Scribed by Donald W. Lewis; Catherine E. Erickson; Frank J. Castora

Book ID
119173589
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
241 KB
Volume
11
Category
Article
ISSN
0887-8994

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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