mtDNA Mutations That Cause Optic Neuropathy: How Do We Know?

Journal article

Open access

Peer reviewed

Neil Howell, Christy Bogolin, Robyn Jamieson, Daniel R Marenda and David A Mackey

American journal of human genetics, v 62(1), pp 196-202

Jan 1998

PMID: 9443868

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https://doi.org/10.1086/301675View

Published, Version of Record (VoR) Open

Leber hereditary optic neuropathy

mtDNA

Mitochondrial disease

Mitochondrial genetics

13 Record Views

50 citations in Scopus

Title: mtDNA Mutations That Cause Optic Neuropathy: How Do We Know?
Creators: Neil Howell - Department of Radiation Oncology, Department of Human Biological Chemistry and Genetics, The University of Texas Medical Branch, Galveston
Christy Bogolin - Department of Radiation Oncology, Department of Human Biological Chemistry and Genetics, The University of Texas Medical Branch, Galveston
Robyn Jamieson - Department of Clinical Genetics, New Children's Hospital, Sydney
Daniel R Marenda - Department of Ophthalmology, University of Iowa, Iowa City
David A Mackey - Departments of Ophthalmology and Paediatrics, The University of Melbourne, Melbourne, and The Menzies Centre, University of Tasmania, Hobart, Australia
Publication Details: American journal of human genetics, v 62(1), pp 196-202
Publisher: Elsevier
Resource Type: Journal article
Language: English
Academic Unit: Biology
Web of Science ID: WOS:000072127900027
Scopus ID: 2-s2.0-0031893037
Other Identifier: 991014878188204721

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