<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

• मुख्य लेखकों: Fischel-Ghodsian Nathan (लेखक), Mercader Josep (लेखक), Ballana Ester (लेखक), Estivill Xavier (लेखक)
• स्वरूप: पुस्तक
• प्रकाशित: BMC, 2007-12-01T00:00:00Z.
• विषय: article
• ऑनलाइन पहुंच: Connect to this object online.

<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...