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. Author manuscript; available in PMC: 2010 Feb 1.
Published in final edited form as: Am J Med Genet A. 2009 Mar;149A(3):555–558. doi: 10.1002/ajmg.a.32670

Fig. 5.

Fig. 5

Domain structure of the RDX gene showing mutations known to cause DFNB24 hearing loss in humans. The novel splice site mutation described in this study (c.698+1G>A) is boxed.