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

פריטים דומים

• Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation
  מאת: Lu, Jianxin, et al.
  יצא לאור: (2009)
• Mitochondrial tRNA(Thr) G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families
  מאת: Wang, Xinjian, et al.
  יצא לאור: (2008)
• Contribution of the tRNA(Ile) 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation
  מאת: Meng, Feilong, et al.
  יצא לאור: (2018)
• Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family
  מאת: Qu, Jia, et al.
  יצא לאור: (2006)
• Aminoglycoside-associated nonsyndromic deafness and speech disorder in mitochondrial A1555G mutation in a family: A case report
  מאת: Ou, Yang-Hao, et al.
  יצא לאור: (2018)