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Ophthalmic Genetics Volume 31, 2010 - Issue 4
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Original Article

Reduced frequency of known mutations in a cohort of LHON patients from India

Periasamy SundaresanDepartment of Genetics, Dr. G. Venkataswamy Eye Research Institute, Aravind Medical Research Foundation, Madurai, Tamilnadu, India
,
S. Mahesh KumarNeuro-ophthalmology Clinic, Aravind Eye Hospital, Madurai, Tamilnadu, India
,
Stewart ThompsonDepartment of Ophthalmology and Visual Sciences, University of Iowa, Iowa City, Iowa, USA
&
John H. FingertDepartment of Ophthalmology and Visual Sciences, University of Iowa, Iowa City, Iowa, USACorrespondence[email protected]
Pages 196-199 | Received 17 Feb 2010, Accepted 17 Jul 2010, Published online: 01 Sep 2010

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. (2012) Abstracts of the 2012 Meeting of the International Neuro-Ophthalmology Society, Singapore. Neuro-Ophthalmology 36:sup1, pages 1-65.
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Articles from other publishers (11)

Manjushree Bhate, Sampada Kulkarni, Rohan Nalawade & Akhilesh Pujar. (2022) Clinical and Genetic Profile of Leber's Hereditary Optic Neuropathy in a Cohort of Patients From a Tertiary Eye Care Center. Journal of Pediatric Ophthalmology & Strabismus 59:5, pages 344-349.
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NaveenKumar Challa, HimaBindu Narsini & Sulaiman Aldakhil. (2022) Phenotypic expressions of chronic leber's hereditary optic neuropathy patients with primary and secondary mitochondrial mutations presenting at tertiary eye care center, South India. Egyptian Retina Journal 9:1, pages 8.
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Vinny Wilson, Prabhjit Kaur, Sofia Singh, RadhikaP Ramachandran, Vislavath Jyothi, KarthikV Mahesh, Aastha Takkar, Giriraj Chandak & Ramandeep Singh. (2022) Clinical profile of patients with leber hereditary optic neuropathy (LHON): An ambispective study of North Indian Cohorts. Annals of Indian Academy of Neurology 25:8, pages 65.
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Srilekha Sundaramurthy, Ambika SelvaKumar, Jared Ching, Vidhya Dharani, Sripriya Sarangapani & Patrick Yu-Wai-Man. (2020) Leber hereditary optic neuropathy—new insights and old challenges. Graefe's Archive for Clinical and Experimental Ophthalmology 259:9, pages 2461-2472.
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Rajan Kumar Jha, Chhavi Dawar, Qurratulain Hasan, Akhilesh Pujar, Gaurav Gupta, Venugopalan Y. Vishnu, Ramesh Kekunnaya & Kumarasamy Thangaraj. (2021) Mitochondrial Genetic Heterogeneity in Leber’s Hereditary Optic Neuropathy: Original Study with Meta-Analysis. Genes 12:9, pages 1300.
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Sunita Mohan, Uthra Satagopan, Soumittra Nagasamy, Sundaram Natarajan & Govindasamy Kumaramanickavel. 2019. Advances in Vision Research, Volume II. Advances in Vision Research, Volume II 147 168 .
Andrew Schaefer, Albert Lim & Grainne Gorman. 2019. Diagnosis and Management of Mitochondrial Disorders. Diagnosis and Management of Mitochondrial Disorders 63 79 .
Bibhuti Ballav Saikia, Sushil Kumar Dubey, Mahesh Kumar Shanmugam & Periasamy Sundaresan. (2017) Whole mitochondrial genome analysis in South Indian patients with Leber's hereditary optic neuropathy. Mitochondrion 36, pages 21-28.
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Anushree Mishra, Saranya Devi, Rohit Saxena, Neerja Gupta, Madhulika Kabra & MadhumitaRoy Chowdhury. (2017) Frequency of primary mutations of Leber's hereditary optic neuropathy patients in North Indian population. Indian Journal of Ophthalmology 65:11, pages 1156.
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Claus Desler & Lene Juel Rasmussen. (2014) Mitochondria in biology and medicine — 2012. Mitochondrion 16, pages 2-6.
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S Iyer, E Xiao, K Alsayegh, N Eroshenko, M J Riggs, J P BennettJrJr & R R Rao. (2011) Mitochondrial gene replacement in human pluripotent stem cell-derived neural progenitors. Gene Therapy 19:5, pages 469-475.
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