000 01890 a2200577 4500
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