000 01582 a2200481 4500
005 20250514001629.0
264 0 _c20010830
008 200108s 0 0 eng d
022 _a1096-7192
024 7 _a10.1006/mgme.2001.3175
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHeil, S G
245 0 0 _aIs mutated serine hydroxymethyltransferase (SHMT) involved in the etiology of neural tube defects?
_h[electronic resource]
260 _bMolecular genetics and metabolism
_cJun 2001
300 _a164-72 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAlleles
650 0 4 _aBase Sequence
650 0 4 _aChild
650 0 4 _aCytosol
_xenzymology
650 0 4 _aDNA Mutational Analysis
650 0 4 _aDNA, Complementary
_xchemistry
650 0 4 _aFemale
650 0 4 _aFolic Acid
_xblood
650 0 4 _aGenotype
650 0 4 _aGlycine Hydroxymethyltransferase
_xgenetics
650 0 4 _aHumans
650 0 4 _aMitochondria
_xenzymology
650 0 4 _aMutation
650 0 4 _aNeural Tube Defects
_xenzymology
650 0 4 _aPolymorphism, Genetic
650 0 4 _aPolymorphism, Single-Stranded Conformational
650 0 4 _aSequence Deletion
700 1 _aVan der Put, N M
700 1 _aWaas, E T
700 1 _aden Heijer, M
700 1 _aTrijbels, F J
700 1 _aBlom, H J
773 0 _tMolecular genetics and metabolism
_gvol. 73
_gno. 2
_gp. 164-72
856 4 0 _uhttps://doi.org/10.1006/mgme.2001.3175
_zAvailable from publisher's website
999 _c11317810
_d11317810