Showing 1 - 5 results of 5 for search 'Scartezini, M', query time: 0.02s
Refine Results
-
1
-
2
DEVELOPMENT OF AN AFFORDABLE, SENSITIVE AND RAPID SCREENING METHOD FOR MUTATION DETECTION IN UK FH SUBJECTS by Scartezini, M, Hubbart, C, Whittall, R, Neil, H, Humphrics, SE
Published 2008Journal article -
3
The PCSK9 gene R46L variant is associated with lower plasma lipid levels and cardiovascular risk in healthy U.K. men. by Scartezini, M, Hubbart, C, Whittall, R, Cooper, J, Neil, A, Humphries, SE
Published 2007Journal article -
4
Development of a high-resolution melting method for mutation detection in familial hypercholesterolaemia patients. by Whittall, R, Scartezini, M, Li, K, Hubbart, C, Reiner, Z, Abraha, A, Neil, H, Dedoussis, G, Humphries, SE
Published 2010Journal article -
5
Healthy individuals carrying the PCSK9 p.R46L variant and familial hypercholesterolemia patients carrying PCSK9 p.D374Y exhibit lower plasma concentrations of PCSK9. by Humphries, SE, Neely, R, Whittall, R, Troutt, J, Konrad, R, Scartezini, M, Li, K, Cooper, J, Acharya, J, Neil, A
Published 2009Journal article