ANALYSIS OF ZNF9 FUNCTION IN CAP-INDEPENDENT TRANSLATION AND MYOTONIC DYSTROPHY TYPE 2
Myotonic dystrophy type 2 (DM2) is an autosomal dominant human disease caused by the expansion of a tetranucleotide repeat in the first intron of the ZNF9 gene. While multiple studies link nucleotide expansions such as those found in the ZNF9 gene to a variety of other human diseases, it is unclear...
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| Format: | Others |
| Language: | en |
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VANDERBILT
2010
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| Online Access: | http://etd.library.vanderbilt.edu/available/etd-08112010-103712/ |