✦ LIBER ✦

Cochlear alterations in deaf and unaffected subjects carrying the deafness-associated A1555G mutation in the mitochondrial 12S rRNA gene

✍ Scribed by Olga Bravo; Ester Ballana; Xavier Estivill

Book ID: 116292683
Publisher: Elsevier Science
Year: 2006
Tongue: English
Weight: 126 KB
Volume: 344
Category: Article
ISSN: 0006-291X
DOI: 10.1016/j.bbrc.2006.03.143

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mitochondrial haplotypes may modulate th

Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation

✍ Jianxin Lu; Yaping Qian; Zhiyuan Li; Aifen Yang; Yi Zhu; Ronghua Li; Li Yang; Xi 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 750 KB

Very low penetrance of hearing loss in s

Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation

✍ Xiaowen Tang; Li Yang; Yi Zhu; Zhisu Liao; Jindan Wang; Yaping Qian; Zhihua Tao; 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 328 KB

53. Mitochondrial tRNAThr G15927A varian

53. Mitochondrial tRNAThr G15927A variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation

✍ Xinjian Wang; Jianxin Lu; Aifen Yang; Li Yang; Yi Zhu; Bobei Chen; Xiaowen Tang; 📂 Article 📅 2009 🏛 Elsevier Science 🌐 English ⚖ 49 KB

Mitochondrial tRNAGlu A14693G variant ma

Mitochondrial tRNAGlu A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family

✍ Yu Ding; Yongyan Li; Junyan You; Li Yang; Bobei Chen; Jianxin Lu; Min-Xin Guan 📂 Article 📅 2009 🏛 Elsevier 🌐 Chinese ⚖ 545 KB

The A1555G Mutation in the 12S rRNA Gene

The A1555G Mutation in the 12S rRNA Gene of Human mtDNA: Recurrent Origins and Founder Events in Families Affected by Sensorineural Deafness

✍ Antonio Torroni; Fulvio Cruciani; Chiara Rengo; Daniele Sellitto; Núria López-Bi 📂 Article 📅 1999 🏛 American Society of Human Genetics 🌐 English ⚖ 107 KB

The ND4 G11696A mutation may influence t

The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family

✍ Zhisu Liao; Jianyue Zhao; Yi Zhu; Li Yang; Aifen Yang; Dongmei Sun; Zhongnong Zh 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 165 KB