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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