Reply: Early-onset Behr syndrome due to compound heterozygous mutations in OPA1

Bibliographic Details
Main Authors: Yu-Wai-Man, Patrick, Chinnery, Patrick F.
Format: Online
Language:English
Published: Oxford University Press 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163031/
id pubmed-4163031
recordtype oai_dc
spelling pubmed-41630312014-09-15 Reply: Early-onset Behr syndrome due to compound heterozygous mutations in OPA1 Yu-Wai-Man, Patrick Chinnery, Patrick F. Letters to the Editor Oxford University Press 2014-10 2014-07-10 /pmc/articles/PMC4163031/ /pubmed/25012222 http://dx.doi.org/10.1093/brain/awu187 Text en © The Author (2014). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Yu-Wai-Man, Patrick
Chinnery, Patrick F.
spellingShingle Yu-Wai-Man, Patrick
Chinnery, Patrick F.
Reply: Early-onset Behr syndrome due to compound heterozygous mutations in OPA1
author_facet Yu-Wai-Man, Patrick
Chinnery, Patrick F.
author_sort Yu-Wai-Man, Patrick
title Reply: Early-onset Behr syndrome due to compound heterozygous mutations in OPA1
title_short Reply: Early-onset Behr syndrome due to compound heterozygous mutations in OPA1
title_full Reply: Early-onset Behr syndrome due to compound heterozygous mutations in OPA1
title_fullStr Reply: Early-onset Behr syndrome due to compound heterozygous mutations in OPA1
title_full_unstemmed Reply: Early-onset Behr syndrome due to compound heterozygous mutations in OPA1
title_sort reply: early-onset behr syndrome due to compound heterozygous mutations in opa1
description
publisher Oxford University Press
publishDate 2014
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163031/
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