Heterozygous OPA1 mutations in Behr syndrome
Author:
Publisher
Oxford University Press (OUP)
Subject
Neurology (clinical)
Link
http://academic.oup.com/brain/article-pdf/134/4/e169/968886/awq306.pdf
Reference10 articles.
1. OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes
2. Sur l'atrophie optique hérédo-familiale compliquée (Behr), forme de passage de l'atrophie de Leber aux hérédo-ataxies; pp. 314–332
3. Type III 3-Methylglutaconic Aciduria (Optic Atrophy Plus Syndrome, or Costeff Optic Atrophy Syndrome): Identification of the OPA3 Gene and Its Founder Mutation in Iraqi Jews
4. Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novelOPA1mutations
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