Co segregation of the m.1555A>G mutation in the MT-RNR1 gene and mutations in MT-ATP6 gene in a family with dilated mitochondrial cardiomyopathy and hearing loss: A whole mitochondrial genome screening-Reference-Cited by-同舟云学术

Co segregation of the m.1555A>G mutation in the MT-RNR1 gene and mutations in MT-ATP6 gene in a family with dilated mitochondrial cardiomyopathy and hearing loss: A whole mitochondrial genome screening

Published:2017-02 Issue:1 Volume:484 Page:71-78
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Alila-Fersi Olfa,Chamkha Imen,Majdoub Imen,Gargouri Lamia,Mkaouar-Rebai Emna,Tabebi Mouna,Tlili Abdelaziz,Keskes Leila,Mahfoudh Abdelmajid,Fakhfakh Faiza

Funder

Ministry of the Higher Education and the Scientific Research in Tunisia

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference40 articles.

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