A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletions-Reference-Cited by-同舟云学术

A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletions

Published:2013-02 Issue:4 Volume:431 Page:670-674
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Mezghani Najla,Mnif Mouna,Mkaouar-Rebai Emna,Kallel Nozha,Charfi Nadia,Abid Mohamed,Fakhfakh Faiza

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference42 articles.

1. Maternally inherited diabetes and deafness: a case report;Maseda;Acta Otorrinolaringol. Esp.,2008

2. Maternally inherited diabetes and deafness: a multicenter study;Guillausseau;Ann. Intern. Med.,2001

3. Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness;Massin;Ophthalmology,1999

4. Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafness;Perucca-Lostanlen;Biochim. Biophys. Acta,2002

5. Prevalence and progression of diabetes in mitochondrial disease;Whittaker;Diabetologia,2007

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mitochondrial complex I subunit MT-ND1 mutations affect disease progression;Heliyon;2024-04

2. A retrospective cohort study evaluating pregnancy outcomes in women with MIDD;Acta Diabetologica;2023-10-31

3. Prevalence and Clinical Characteristics of Mitochondrial DNA Mutations in Korean Patients With Sensorineural Hearing Loss;Journal of Korean Medical Science;2023

4. Nanotechnology to Correct Mitochondrial Disorders in Cancer Diseases;Cancer Nanotechnology;2022-12-14

5. Leigh Syndrome in a Pedigree Harboring the m.1555A>G Mutation in the Mitochondrial 12S rRNA;Genes;2020-08-27