A novel de novo dominant mutation in ISCU associated with mitochondrial myopathy (2017)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1136/jmedgenet-2017-104822
Publication URI: http://dx.doi.org/10.1136/jmedgenet-2017-104822
Type: Journal Article/Review
Parent Publication: Journal of Medical Genetics
Issue: 12