Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss-Reference-Cited by-同舟云学术

Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss

Published:2010-09 Issue:9 Volume:74 Page:1071-1074
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Nahili Halima,Charif Majida,Boulouiz Redouane,bounaceur Safaa,Benrahma Houda,Abidi Omar,Chafik Abdelaziz,Rouba Hassan,Kandil Mostafa,Barakat Abdelhamid

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference31 articles.

1. Symposium on sensorineural hearing loss in children: early detection and intervention. Genetic factors in deafness of early life;Nance;Otolaryngol. Clin. N. Am.,1975

2. Genetic epidemiology of hearing impairment;Morton;Ann. N. Y. Acad. Sci.,1991

3. Molecular genetics of hearing loss;Petit;Annu. Rev. Genet.,2001

4. Genetics, genomics and gene discovery in the auditory system;Morton;Hum. Mol. Genet.,2002

5. Mitochondrial deafness mutations reviewed;Fischel-Ghodsian;Hum. Mutat.,1999

Cited by 16 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. mtDNA Single-Nucleotide Variants Associated with Type 2 Diabetes;Current Issues in Molecular Biology;2023-10-30

2. Crucial Roles of the m.1555A>G Mutation on MT-RNR1 Gene in Hearing Loss;J BIOL REG HOMEOS AG;2022

3. Hearing loss in Africa: current genetic profile;Human Genetics;2021-10-05

4. Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family;Human Heredity;2021-01-22

5. Genetic Epidemiology of Hearing Loss in the 22 Arab Countries: A Systematic Review;Otology & Neurotology;2020-02