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Familial partial lipodystrophy due to the LMNA R482W mutation with multinodular goitre, extrapyramidal syndrome and primary hyperaldosteronism
M. C. Vantyghem, F. Faivre-Defrance, S. Marcelli-Tourvieille, C. Fermon, A. Evrard, M. F. Bourdelle-Hego, C. Vigouroux, L. Defebvre, B. Delemer, J. L. WemeauVolume:
67
Year:
2007
Language:
english
Pages:
3
DOI:
10.1111/j.1365-2265.2007.02870.x
File:
PDF, 85 KB
english, 2007