Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss

مواد مشابهة

• Uniparental disomy of chromosome 13q causing homozygosity for the 35delG mutation in the gene encoding connexin26 (GJB2) results in prelingual hearing impairment in two unrelated Spanish patients
  بواسطة: Alvarez, A, وآخرون
  منشور في: (2003)
• Q829X, a novel mutation in the gene encoding otoferlin (OTOF), is frequently found in Spanish patients with prelingual non-syndromic hearing loss
  بواسطة: Migliosi, V, وآخرون
  منشور في: (2002)
• Maternally inherited non-syndromic hearing impairment in a Spanish family with the 7510T>C mutation in the mitochondrial tRNA(Ser(UCN)) gene
  بواسطة: del Castillo, F J, وآخرون
  منشور في: (2002)
• Molecular and clinical characterisation of three Spanish families with maternally inherited non‐syndromic hearing loss caused by the 1494C→T mutation in the mitochondrial 12S rRNA gene
  بواسطة: Rodríguez‐Ballesteros, M, وآخرون
  منشور في: (2006)
• Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation
  بواسطة: Zhu, Yuhua, وآخرون
  منشور في: (2014)