| 000 | 01386 a2200421 4500 | ||
|---|---|---|---|
| 005 | 20250515112712.0 | ||
| 264 | 0 | _c20080918 | |
| 008 | 200809s 0 0 eng d | ||
| 022 | _a1432-0584 | ||
| 024 | 7 |
_a10.1007/s00277-008-0465-0 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aRemacha, A F | |
| 245 | 0 | 0 |
_aRole of (Glu --> Arg, Q5R) mutation of the intrinsic factor in pernicious anemia and other causes of low vitamin B12. _h[electronic resource] |
| 260 |
_bAnnals of hematology _cJul 2008 |
||
| 300 |
_a599-600 p. _bdigital |
||
| 500 | _aPublication Type: Letter | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAmino Acid Substitution |
| 650 | 0 | 4 |
_aAnemia, Pernicious _xgenetics |
| 650 | 0 | 4 |
_aGastric Mucosa _xmetabolism |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIntestinal Absorption |
| 650 | 0 | 4 |
_aIntrinsic Factor _xgenetics |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 | _aPoint Mutation |
| 650 | 0 | 4 | _aRisk |
| 650 | 0 | 4 |
_aVitamin B 12 _xpharmacokinetics |
| 650 | 0 | 4 |
_aVitamin B 12 Deficiency _xgenetics |
| 700 | 1 | _aDel Río, E | |
| 700 | 1 | _aSardà, M P | |
| 700 | 1 | _aCanals, C | |
| 700 | 1 | _aSimó, M | |
| 700 | 1 | _aBaiget, M | |
| 773 | 0 |
_tAnnals of hematology _gvol. 87 _gno. 7 _gp. 599-600 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s00277-008-0465-0 _zAvailable from publisher's website |
| 999 |
_c17839919 _d17839919 |
||