| 000 | 01147 a2200301 4500 | ||
|---|---|---|---|
| 005 | 20250516025714.0 | ||
| 264 | 0 | _c20111202 | |
| 008 | 201112s 0 0 eng d | ||
| 022 | _a1573-2665 | ||
| 024 | 7 |
_a10.1007/s10545-011-9301-0 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aCantagrel, Vincent | |
| 245 | 0 | 0 |
_aFrom glycosylation disorders to dolichol biosynthesis defects: a new class of metabolic diseases. _h[electronic resource] |
| 260 |
_bJournal of inherited metabolic disease _cAug 2011 |
||
| 300 |
_a859-67 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Review | ||
| 650 | 0 | 4 | _aAnimals |
| 650 | 0 | 4 |
_aCongenital Disorders of Glycosylation _xclassification |
| 650 | 0 | 4 |
_aDolichols _xbiosynthesis |
| 650 | 0 | 4 | _aGlycosylation |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aMetabolic Diseases _xclassification |
| 650 | 0 | 4 | _aModels, Biological |
| 650 | 0 | 4 |
_aProtein Processing, Post-Translational _xgenetics |
| 700 | 1 | _aLefeber, Dirk J | |
| 773 | 0 |
_tJournal of inherited metabolic disease _gvol. 34 _gno. 4 _gp. 859-67 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s10545-011-9301-0 _zAvailable from publisher's website |
| 999 |
_c20656734 _d20656734 |
||