000 01358 a2200385 4500
005 20250514065832.0
264 0 _c20040130
008 200401s 0 0 eng d
022 _a1552-4825
024 7 _a10.1002/ajmg.a.20115
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMorin, Isabelle
245 0 0 _aCommon variant in betaine-homocysteine methyltransferase (BHMT) and risk for spina bifida.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cJun 2003
300 _a172-6 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 _aAmino Acid Substitution
650 0 4 _aBetaine-Homocysteine S-Methyltransferase
650 0 4 _aFemale
650 0 4 _aGenetic Variation
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMethyltransferases
_xgenetics
650 0 4 _aPoint Mutation
650 0 4 _aSpinal Dysraphism
_xgenetics
700 1 _aPlatt, Robert
700 1 _aWeisberg, Ilan
700 1 _aSabbaghian, Nelly
700 1 _aWu, Qing
700 1 _aGarrow, Timothy A
700 1 _aRozen, Rima
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 119A
_gno. 2
_gp. 172-6
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.20115
_zAvailable from publisher's website
999 _c12537406
_d12537406