<it>MRPS18CP2 </it>alleles and <it>DEFA3 </it>absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene
<p>Abstract</p> <p>Background</p> <p>Mitochondrial DNA (mtDNA) mutations account for at least 5% of cases of postlingual, nonsyndromic hearing impairment. Among them, mutation A1555G is frequently found associated with aminoglycoside-induced and/or nonsyndromic hearing...
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| Main Authors: | , , , |
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| Format: | Book |
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BMC,
2007-12-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |