Mutational screening in patients with profound sensorineural hearing loss and neurodevelopmental delay: Description of a novel m.3861A > C mitochondrial mutation in the MT-ND1 gene-Reference-Cited by-同舟云学术

Mutational screening in patients with profound sensorineural hearing loss and neurodevelopmental delay: Description of a novel m.3861A > C mitochondrial mutation in the MT-ND1 gene

Published:2016-06 Issue:4 Volume:474 Page:702-708
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Ammar Marwa,Tabebi Mouna,Sfaihi Lamia,Alila-Fersi Olfa,Maalej Marwa,Felhi Rahma,Chabchoub Imen,Keskes Leila,Hachicha Mongia,Fakhfakh Faiza,Mkaouar-Rebai Emna

Funder

Ministry of Higher Education

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

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5. The spectrum of hearing loss due to mitochondrial DNA defects

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