| 000 | 01856 a2200553 4500 | ||
|---|---|---|---|
| 005 | 20250514182514.0 | ||
| 264 | 0 | _c20040506 | |
| 008 | 200405s 0 0 eng d | ||
| 022 | _a1098-1004 | ||
| 024 | 7 |
_a10.1002/humu.20014 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aTanner, Stephan M | |
| 245 | 0 | 0 |
_aGenetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East. _h[electronic resource] |
| 260 |
_bHuman mutation _cApr 2004 |
||
| 300 |
_a327-33 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. | ||
| 650 | 0 | 4 |
_aAnemia, Megaloblastic _xgenetics |
| 650 | 0 | 4 | _aConsanguinity |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aFounder Effect |
| 650 | 0 | 4 | _aHaplotypes |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIntestinal Absorption |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMembrane Proteins |
| 650 | 0 | 4 | _aMiddle East |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 |
_aProteins _xgenetics |
| 650 | 0 | 4 |
_aReceptors, Cell Surface _xgenetics |
| 650 | 0 | 4 | _aScandinavian and Nordic Countries |
| 650 | 0 | 4 |
_aVitamin B 12 Deficiency _xdiagnosis |
| 700 | 1 | _aLi, Zhongyuan | |
| 700 | 1 | _aBisson, Ryan | |
| 700 | 1 | _aAcar, Ceren | |
| 700 | 1 | _aOner, Cihan | |
| 700 | 1 | _aOner, Reyhan | |
| 700 | 1 | _aCetin, Mualla | |
| 700 | 1 | _aAbdelaal, Mohamed A | |
| 700 | 1 | _aIsmail, Essam A | |
| 700 | 1 | _aLissens, Willy | |
| 700 | 1 | _aKrahe, Ralf | |
| 700 | 1 | _aBroch, Harald | |
| 700 | 1 | _aGräsbeck, Ralph | |
| 700 | 1 | _ade la Chapelle, Albert | |
| 773 | 0 |
_tHuman mutation _gvol. 23 _gno. 4 _gp. 327-33 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/humu.20014 _zAvailable from publisher's website |
| 999 |
_c14743000 _d14743000 |
||