000 01124 a2200301 4500
005 20250513114308.0
264 0 _c19970626
008 199706s 0 0 eng d
022 _a1059-7794
024 7 _a10.1002/(SICI)1098-1004(1997)9:4<291::AID-HUMU1>3.0.CO;2-9
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSt-Louis, M
245 0 0 _aMutations in the fumarylacetoacetate hydrolase gene causing hereditary tyrosinemia type I: overview.
_h[electronic resource]
260 _bHuman mutation
_c1997
300 _a291-9 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
650 0 4 _aAmino Acid Metabolism, Inborn Errors
_xgenetics
650 0 4 _aAnimals
650 0 4 _aDisease Models, Animal
650 0 4 _aHumans
650 0 4 _aHydrolases
_xgenetics
650 0 4 _aMice
650 0 4 _aMutation
_xgenetics
650 0 4 _aTyrosine
_xmetabolism
700 1 _aTanguay, R M
773 0 _tHuman mutation
_gvol. 9
_gno. 4
_gp. 291-9
856 4 0 _uhttps://doi.org/10.1002/(SICI)1098-1004(1997)9:4<291::AID-HUMU1>3.0.CO;2-9
_zAvailable from publisher's website
999 _c9083746
_d9083746