Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients. (2014)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1186/s13023-014-0119-3
PubMed Identifier: 25208612
Publication URI: http://europepmc.org/abstract/MED/25208612
Type: Journal Article/Review
Volume: 9
Parent Publication: Orphanet journal of rare diseases
ISSN: 1750-1172