000 01349 a2200421 4500
005 20250515172910.0
264 0 _c20090813
008 200908s 0 0 eng d
022 _a1098-1004
024 7 _a10.1002/humu.21021
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aWilliams, Emma L
245 0 0 _aPrimary hyperoxaluria type 1: update and additional mutation analysis of the AGXT gene.
_h[electronic resource]
260 _bHuman mutation
_cJun 2009
300 _a910-7 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aAlleles
650 0 4 _aAnimals
650 0 4 _aDNA Mutational Analysis
650 0 4 _aHumans
650 0 4 _aHyperoxaluria, Primary
_xdiagnosis
650 0 4 _aPolymorphism, Genetic
650 0 4 _aTransaminases
_xchemistry
650 0 4 _aUniparental Disomy
_xgenetics
700 1 _aAcquaviva, Cecile
700 1 _aAmoroso, Antonio
700 1 _aChevalier, Francoise
700 1 _aCoulter-Mackie, Marion
700 1 _aMonico, Carla G
700 1 _aGiachino, Daniela
700 1 _aOwen, Tricia
700 1 _aRobbiano, Angela
700 1 _aSalido, Eduardo
700 1 _aWaterham, Hans
700 1 _aRumsby, Gill
773 0 _tHuman mutation
_gvol. 30
_gno. 6
_gp. 910-7
856 4 0 _uhttps://doi.org/10.1002/humu.21021
_zAvailable from publisher's website
999 _c18905030
_d18905030