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

  Raffan, Eleanor

Stewart, CL

  O'Rahilly, Stephen

  Semple, Robert

Raef, H

Rochford, Justin

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Publication Date

2013-01

Journal 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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Citation

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



Rights

Attribution 4.0 International

Licence URL: https://creativecommons.org/licenses/by/4.0/