000 | 00839 a2200289 4500 | ||
---|---|---|---|
005 | 20250515020116.0 | ||
264 | 0 | _c20060321 | |
008 | 200603s 0 0 eng d | ||
022 | _a0340-6717 | ||
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aArranz, A | |
245 | 0 | 0 |
_aGene symbol: FAH. Disease: tyrosinaemia 1. _h[electronic resource] |
260 |
_bHuman genetics _cDec 2005 |
||
300 |
_a537 p. _bdigital |
||
500 | _aPublication Type: Journal Article | ||
650 | 0 | 4 | _aAmino Acid Substitution |
650 | 0 | 4 | _aCodon, Nonsense |
650 | 0 | 4 | _aDNA Mutational Analysis |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aHydrolases _xgenetics |
650 | 0 | 4 | _aMutation, Missense |
650 | 0 | 4 |
_aTyrosinemias _xgenetics |
700 | 1 | _aRigante, D | |
700 | 1 | _aAntuzzi, D | |
700 | 1 | _aRiudor, E | |
773 | 0 |
_tHuman genetics _gvol. 118 _gno. 3-4 _gp. 537 |
|
999 |
_c16130950 _d16130950 |