| 000 | 01463 a2200421 4500 | ||
|---|---|---|---|
| 005 | 20250514182355.0 | ||
| 264 | 0 | _c20040604 | |
| 008 | 200406s 0 0 eng d | ||
| 022 | _a0021-9150 | ||
| 024 | 7 |
_a10.1016/j.atherosclerosis.2003.11.011 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aTremblay, André J | |
| 245 | 0 | 0 |
_aLack of evidence for reduced plasma apo B48 catabolism in patients with heterozygous familial hypercholesterolemia carrying the same null LDL receptor gene mutation. _h[electronic resource] |
| 260 |
_bAtherosclerosis _cFeb 2004 |
||
| 300 |
_a367-73 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aApolipoprotein B-48 |
| 650 | 0 | 4 |
_aApolipoproteins B _xblood |
| 650 | 0 | 4 | _aChylomicron Remnants |
| 650 | 0 | 4 |
_aChylomicrons _xmetabolism |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHyperlipoproteinemia Type II _xblood |
| 650 | 0 | 4 | _aIsotopes |
| 650 | 0 | 4 | _aLeucine |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aReceptors, LDL _xgenetics |
| 700 | 1 | _aLamarche, Benoît | |
| 700 | 1 | _aRuel, Isabelle | |
| 700 | 1 | _aHogue, Jean-Charles | |
| 700 | 1 | _aBergeron, Jean | |
| 700 | 1 | _aGagné, Claude | |
| 700 | 1 | _aCouture, Patrick | |
| 773 | 0 |
_tAtherosclerosis _gvol. 172 _gno. 2 _gp. 367-73 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.atherosclerosis.2003.11.011 _zAvailable from publisher's website |
| 999 |
_c14738938 _d14738938 |
||