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 |