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Heterozygous OPA1 mutations in Behr syndrome.

Authors :
Marelli C
Amati-Bonneau P
Reynier P
Layet V
Layet A
Stevanin G
Brissaud E
Bonneau D
Durr A
Brice A
Source :
Brain : a journal of neurology [Brain] 2011 Apr; Vol. 134 (Pt 4), pp. e169; author reply e170. Date of Electronic Publication: 2010 Nov 26.
Publication Year :
2011

Subjects

Subjects :
Ataxia genetics
Hearing Loss genetics
Humans
Intellectual Disability genetics
Mutation
Optic Atrophy congenital
Optic Atrophy genetics
Spasm genetics
GTP Phosphohydrolases genetics

Details

Language :
English
ISSN :
1460-2156
Volume :
134
Issue :
Pt 4
Database :
MEDLINE
Journal :
Brain : a journal of neurology
Publication Type :
Report
Accession number :
21112924
Full Text :
https://doi.org/10.1093/brain/awq306
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