| 000 | 01345 a2200373 4500 | ||
|---|---|---|---|
| 005 | 20250512081220.0 | ||
| 264 | 0 | _c19870109 | |
| 008 | 198701s 0 0 eng d | ||
| 022 | _a0141-8955 | ||
| 024 | 7 |
_a10.1007/BF01801665 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aAugereau, C | |
| 245 | 0 | 0 |
_aPyruvate carboxylase deficiencies: complementation studies between "French" and "American" phenotypes in cultured fibroblasts. _h[electronic resource] |
| 260 |
_bJournal of inherited metabolic disease _c1985 |
||
| 300 |
_a59-62 p. _bdigital |
||
| 500 | _aPublication Type: Comparative Study; Journal Article | ||
| 650 | 0 | 4 |
_aAmino Acid Metabolism, Inborn Errors _xgenetics |
| 650 | 0 | 4 | _aCells, Cultured |
| 650 | 0 | 4 |
_aFibroblasts _xenzymology |
| 650 | 0 | 4 | _aGenetic Complementation Test |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aMultiple Carboxylase Deficiency _xgenetics |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aPyruvate Carboxylase _xgenetics |
| 650 | 0 | 4 | _aPyruvate Carboxylase Deficiency Disease |
| 700 | 1 | _aPham Dinh, D | |
| 700 | 1 | _aMoncion, A | |
| 700 | 1 | _aMarsac, C | |
| 700 | 1 | _aSaudubray, J M | |
| 700 | 1 | _aRobinson, B H | |
| 773 | 0 |
_tJournal of inherited metabolic disease _gvol. 8 _gno. 2 _gp. 59-62 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/BF01801665 _zAvailable from publisher's website |
| 999 |
_c3945217 _d3945217 |
||