000 01514 a2200493 4500
005 20250517215003.0
264 0 _c20190710
008 201907s 0 0 eng d
022 _a1528-0020
024 7 _a10.1182/blood-2018-03-841023
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHu, Yao
245 0 0 _aA common
_h[electronic resource]
260 _bBlood
_c06 2018
300 _a2859-2863 p.
_bdigital
500 _aPublication Type: Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
650 0 4 _aBlack or African American
_xgenetics
650 0 4 _aFemale
650 0 4 _aGenome-Wide Association Study
650 0 4 _aHumans
650 0 4 _aLoss of Function Mutation
650 0 4 _aMale
650 0 4 _aPolymorphism, Single Nucleotide
650 0 4 _aTranscobalamins
_xgenetics
650 0 4 _aVitamin B 12
_xblood
650 0 4 _aVitamin B Deficiency
_xblood
700 1 _aRaffield, Laura M
700 1 _aPolfus, Linda M
700 1 _aMoscati, Arden
700 1 _aNadkarni, Girish
700 1 _aPreuss, Michael H
700 1 _aZhong, Xue
700 1 _aWei, Qiang
700 1 _aRich, Stephen S
700 1 _aLi, Yun
700 1 _aWilson, James G
700 1 _aCorrea, Adolfo
700 1 _aLoos, Ruth J F
700 1 _aLi, Bingshan
700 1 _aAuer, Paul L
700 1 _aReiner, Alex P
773 0 _tBlood
_gvol. 131
_gno. 25
_gp. 2859-2863
856 4 0 _uhttps://doi.org/10.1182/blood-2018-03-841023
_zAvailable from publisher's website
999 _c28394654
_d28394654