Atypical Presentation of Leber's Hereditary Optic Neuropathy Associated to Mtdna 11778G > A Point Mutation - A Case Report

AuthID
 P-004-BD4
7
Author(s)
Robalo, CB
·
Document Type
Article
Year published
2007
Published
in EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, ISSN: 1090-3798
Volume: 11, Issue: 2, Pages: 115-118 (4)
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Wos®
Scopus®
Crossref®17
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 17254817
SCOPUS: 2-s2.0-33847234224
Wos: WOS:000245208200010
Source Identifiers
ISSN: 1090-3798
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