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

Subjects

Subjects :

*GENETIC mutation
*FRIEDREICH'S ataxia
*ATAXIA
*PERIPHERAL neuropathy
*MITOCHONDRIAL DNA
*PHENOTYPES

Details

Language :

English

ISSN :

00068950

Volume :

137

Issue :

10

Database :

Academic Search Index

Journal :

Brain: A Journal of Neurology

Publication Type :

Academic Journal

Accession number :

98635295

Full Text :

https://doi.org/10.1093/brain/awu184