A novel MT-CO1 m.6498C>A variation associated with the m.7444G>A mutation in the mitochondrial COI/tRNASer(UCN) genes in a patient with hearing impairment, diabetes and congenital visual loss
Mkaouar-Rebai, Emna, Chamkha, Imen, Kammoun, Thouraya, Alila-Fersi, Olfa, Aloulou, Hajer, Hachicha, Mongia, Fakhfakh, FaizaVolume:
430
Language:
english
Journal:
Biochemical and Biophysical Research Communications
DOI:
10.1016/j.bbrc.2012.11.109
Date:
January, 2013
File:
PDF, 1.26 MB
english, 2013