Ramanathan, N., Ahmed, M., Raffan, E., Stewart, C. L., O’Rahilly, S., Semple, R. K., . . . Rochford, J. J. (2012). Identification and Characterisation of a Novel Pathogenic Mutation in the Human Lipodystrophy Gene AGPAT2: C48R: A Novel Mutation in AGPAT2. Springer Berlin Heidelberg.

Ramanathan, N., M. Ahmed, E. Raffan, C. L. Stewart, S. O’Rahilly, R. K. Semple, H. Raef, ja J. J. Rochford. Identification and Characterisation of a Novel Pathogenic Mutation in the Human Lipodystrophy Gene AGPAT2: C48R: A Novel Mutation in AGPAT2. Springer Berlin Heidelberg, 2012.

Ramanathan, N., et al. Identification and Characterisation of a Novel Pathogenic Mutation in the Human Lipodystrophy Gene AGPAT2: C48R: A Novel Mutation in AGPAT2. Springer Berlin Heidelberg, 2012.