A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia.
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- Clinical Genetics, 2009, v. 75, n. 6, p. 562, doi. 10.1111/j.1399-0004.2009.01183.x
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Works matching AU Akay, H. Öztürkmen
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Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.
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- Clinical Genetics, 2008, v. 73, n. 6, p. 554, doi. 10.1111/j.1399-0004.2008.01004.x
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