000 | 01890 a2200577 4500 | ||
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005 | 20250516231335.0 | ||
264 | 0 | _c20150311 | |
008 | 201503s 0 0 eng d | ||
022 | _a1365-2141 | ||
024 | 7 |
_a10.1111/bjh.13078 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aPoulain, Stéphanie | |
245 | 0 | 0 |
_aMYD88 L265P mutation contributes to the diagnosis of Bing Neel syndrome. _h[electronic resource] |
260 |
_bBritish journal of haematology _cNov 2014 |
||
300 |
_a506-13 p. _bdigital |
||
500 | _aPublication Type: Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aAged |
650 | 0 | 4 |
_aBone Marrow _xmetabolism |
650 | 0 | 4 | _aHeterozygote |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMiddle Aged |
650 | 0 | 4 | _aMutation, Missense |
650 | 0 | 4 |
_aMyeloid Differentiation Factor 88 _xgenetics |
650 | 0 | 4 |
_aNeoplasm Proteins _xgenetics |
650 | 0 | 4 |
_aNervous System Diseases _xcerebrospinal fluid |
650 | 0 | 4 | _aProspective Studies |
650 | 0 | 4 | _aSyndrome |
650 | 0 | 4 |
_aWaldenstrom Macroglobulinemia _xcerebrospinal fluid |
700 | 1 | _aBoyle, Eileen M | |
700 | 1 | _aRoumier, Christophe | |
700 | 1 | _aDemarquette, Hélène | |
700 | 1 | _aWemeau, Mathieu | |
700 | 1 | _aGeffroy, Sandrine | |
700 | 1 | _aHerbaux, Charles | |
700 | 1 | _aBertrand, Elisabeth | |
700 | 1 | _aHivert, Bénédicte | |
700 | 1 | _aTerriou, Louis | |
700 | 1 | _aVerrier, Albert | |
700 | 1 | _aPollet, Jean Paul | |
700 | 1 | _aMaurage, Claude Alain | |
700 | 1 | _aOnraed, Brigitte | |
700 | 1 | _aMorschhauser, Franck | |
700 | 1 | _aQuesnel, Bruno | |
700 | 1 | _aDuthilleul, Patrick | |
700 | 1 | _aPreudhomme, Claude | |
700 | 1 | _aLeleu, Xavier | |
773 | 0 |
_tBritish journal of haematology _gvol. 167 _gno. 4 _gp. 506-13 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1111/bjh.13078 _zAvailable from publisher's website |
999 |
_c24133453 _d24133453 |