![](/img/cover-not-exists.png)
A novel LCAT mutation (Phe382→Val) in a kindred with familial LCAT deficiency and defective apolipoprotein B-100
M.Nazeem Nanjee, Joseph Stocks, C.Justin Cooke, Henri O.F Molhuizen, Santica Marcovina, David Crook, John P Kastelein, Norman E MillerVolume:
170
Year:
2003
Language:
english
DOI:
10.1016/s0021-9150(03)00241-7
File:
PDF, 259 KB
english, 2003