Familial hypercholesterolaemia: a global call to arms

Familial Hypercholesterolaemia (FH) is the commonest autosomal co-dominantly inherited condition affecting man. It is caused by mutation in one of three genes, encoding the low-density lipoprotein (LDL) receptor, or the gene for apolipoprotein B (which is the major protein component of the LDL parti...

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Main Author: Vallejo-Vaz, A.J. (author)
Other Authors: Kondapally Seshasai, S.R. (author), Cole, D. (author), Hovingh, G.K. (author), Kastelein, J.J. (author), Mata, P. (author), Raal, F.J. (author), Santos, R.D. (author), Soran, H. (author), Watts, G.F. (author), Abifadel, M. (author), Aguilar-Salinas, C.A. (author), Akram, A. (author), Alnouri, F. (author), Alonso, R. (author), Al-Rasadi, K. (author), Banach, M. (author), Bogsrud, M.P. (author), Bourbon, M. (author), Bruckert, E. (author), Car, J. (author), Corral, P. (author), Descamps, O. (author), Dieplinger, H. (author), Durst, R. (author), Freiberger, T. (author), Gaspar, I.M. (author), Genest, J. (author), Harada-Shiba, M. (author), Jiang, L. (author), Kayikcioglu, M. (author), Lam, C.S. (author), Latkovskis, G. (author), Laufs, U. (author), Liberopoulos, E. (author), Nilsson, L. (author), Nordestgaard, B.G. (author), O'Donoghue, J.M. (author), Sahebkar, A. (author), Schunkert, H. (author), Shehab, A. (author), Stoll, M. (author), Su, TC (author), Susekov, A. (author), Widén, E. (author), Catapano, A.L. (author), Ray, K.K. (author)
Format: article
Language:eng
Published: 2015
Subjects:
Familial Hypercholesterolaemia
Doenças Cardio e Cérebro-vasculares
Online Access:http://hdl.handle.net/10400.18/3174
Country:Portugal
Oai:oai:repositorio.insa.pt:10400.18/3174

Internet

http://hdl.handle.net/10400.18/3174

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