Identification and Characterisation of a Novel Pathogenic Mutation in the Human Lipodystrophy Gene AGPAT2 : C48R: A Novel Mutation in AGPAT2.
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Authors
Ramanathan, N
Ahmed, M
Stewart, CL
Raef, H
Rochford, Justin
Publication Date
2013-01Journal Title
JIMD reports
ISSN
2192-8304
Volume
9
Pages
73-80
Language
eng
Type
Article
This Version
VoR
Physical Medium
Print-Electronic
Metadata
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Ramanathan, N., Ahmed, M., Raffan, E., Stewart, C., O'Rahilly, S., Semple, R., Raef, H., & et al. (2013). Identification and Characterisation of a Novel Pathogenic Mutation in the Human Lipodystrophy Gene AGPAT2 : C48R: A Novel Mutation in AGPAT2.. JIMD reports, 9 73-80. https://doi.org/10.1007/8904_2012_181
Sponsorship
MRC (G0800203)
MRC (G0600717B)
Medical Research Council (MC_UU_12012/5/B)
Wellcome Trust (078986/Z/06/Z)
Wellcome Trust (080952/Z/06/Z)
Wellcome Trust (087678/Z/08/Z)
Wellcome Trust (095515/Z/11/Z)
Wellcome Trust (098498/Z/12/Z)
Identifiers
External DOI: https://doi.org/10.1007/8904_2012_181
This record's URL: https://www.repository.cam.ac.uk/handle/1810/301762