Analysis of mitochondrial A1555G mutation in infants with hearing impairment-Reference-Cited by-同舟云学术

Analysis of mitochondrial A1555G mutation in infants with hearing impairment

Published:2018-04-18 Issue: Volume: Page:
ISSN:1792-0981
Container-title:Experimental and Therapeutic Medicine
language:
Short-container-title:Exp Ther Med

Author:

Wu Lihua¹,Li Ruiyu¹,Chen Juan¹,Chen Yanping²,Yang Meijun³,Wu Qing⁴

Affiliation:

1. Department of Otolaryngology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, Fujian 350001, P.R. China

2. Department of Obstetrics, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, Fujian 350001, P.R. China

3. Department of Neonatology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, Fujian 350001, P.R. China

4. Department of Neonatology, Fujian Provincial Maternal and Child Health Care Hospital, Fuzhou, Fujian 350001, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Immunology and Microbiology (miscellaneous),General Medicine

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1. Evaluation of nephrotoxicity and ototoxicity following amikacin administration once daily or every 48 hours in neonates;Medicine;2022-10-28

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

3. Mutational Analysis of Mitochondrial tRNA Genes in 200 Patients with Type 2 Diabetes Mellitus;International Journal of General Medicine;2021-09

4. Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment;Experimental Biology and Medicine;2020-09-30

5. Low penetrance of hearing loss in two Chinese families carrying the mitochondrial tRNASer(UCN) mutations;Molecular Medicine Reports;2020-04-30