High frequency of the IVS2-2A>G DNA sequence variation in SLC26A5, encoding the cochlear motor protein prestin, precludes its involvement in hereditary hearing loss.
| Autor: | Hsiao-Yuan Tang1 tang@bcm.tmc.edu, Anping Xia1 axia@bcm.tmc.edu, Oghalai, John S1 jso@bcm.tmc.edu, Pereira, Fred A1,2 fpereira@bcm.tmc.edu, Alford, Raye L1 ralford@bcm.tmc.edu |
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| Zdroj: | BMC Medical Genetics. 2005, Vol. 6, p1-7. 7p. 1 Diagram, 3 Charts. |
| Databáze: | Academic Search Ultimate |
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