Complete Mitochondrial Genome Analysis and Clinical Documentation of a Five-Generational Indian Family with Mitochondrial 1555A>G Mutation and Postlingual Hearing Loss-Reference-Cited by-同舟云学术

Complete Mitochondrial Genome Analysis and Clinical Documentation of a Five-Generational Indian Family with Mitochondrial 1555A>G Mutation and Postlingual Hearing Loss

Published:2014-03-24 Issue:3 Volume:78 Page:217-234
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Annals of Human Genetics

Author:

Subathra Mahalingam¹,Selvakumari Mathiyalagan¹,Ramesh Arabandi¹,Ramakrishnan Rajagopalan²,Karan Kalpita Rashmi³,Kaur Manpreet³,Manikandan Mayakannan¹,Srikumari Srisailapathy C. R.¹

Affiliation:

1. Department of Genetics; Dr. ALM Post Graduate Institute of Basic Medical Sciences; University of Madras; Taramani Campus Chennai India

2. Department of ENT; SRM Medical College Hospital and Research Centre; SRM University; Potheri Kattankulathur India

3. Molecular Biology and Genetics Unit; Jawaharlal Nehru Centre for Advanced Scientific Research; Jakkur Bengaluru India

Funder

University Grants Commission

University Industry Community Interaction Centre (UICIC) - University of Madras funds

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ahg.12061/fullpdf

Reference66 articles.

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2. Leber's hereditary optic neuropathy: The mitochondrial connection revisited;Abu-Amero;Middle East Afr J Ophthalmol,2011

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4. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA;Andrews;Nat Genet,1999

5. Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation;Bae;PLoS One,2012

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

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