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-Reference-Cited by-同舟云学术

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

Published:2013-01 Issue:2 Volume:430 Page:585-591
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Mkaouar-Rebai Emna,Chamkha Imen,Kammoun Thouraya,Alila-Fersi Olfa,Aloulou Hajer,Hachicha Mongia,Fakhfakh Faiza

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

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