Review on the functions of Rasd1 interacting proteins.
Smith-Magenis syndrome (SMS) is a genetic disease associated with an interstitial deletion of band p11.2 on chromosome 17. Rasd1 is one of the genes in the minimum deletion interval necessary to produce the SMS phenotype. Besides being a non-receptor activator of G-protein signaling in mammalian cel...
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| Format: | Final Year Project (FYP) |
| Language: | English |
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2009
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| Online Access: | http://hdl.handle.net/10356/15456 |