000 01348 a2200433 4500
005 20250514142213.0
264 0 _c19961201
008 199612s 0 0 eng d
022 _a0140-6736
024 7 _a10.1016/s0140-6736(64)92605-4
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKOPELMAN, H
245 0 0 _aHYPERPROLINAEMIA AND HEREDITARY NEPHRITIS.
_h[electronic resource]
260 _bLancet (London, England)
_cNov 1964
300 _a1075-9 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _a1-Pyrroline-5-Carboxylate Dehydrogenase
_xdeficiency
650 0 4 _aAmino Acid Metabolism, Inborn Errors
650 0 4 _aBlood
650 0 4 _aBlood Chemical Analysis
650 0 4 _aChromatography
650 0 4 _aDiseases in Twins
650 0 4 _aFluids and Secretions
650 0 4 _aGenetics, Medical
650 0 4 _aGlycine
650 0 4 _aHumans
650 0 4 _aHydroxyproline
650 0 4 _aNephritis, Hereditary
650 0 4 _aNephrotic Syndrome
650 0 4 _aPathology
650 0 4 _aProline
650 0 4 _aProline Oxidase
650 0 4 _aProteinuria
650 0 4 _aUrine
700 1 _aASATOOR, A M
700 1 _aMILNE, M D
773 0 _tLancet (London, England)
_gvol. 2
_gno. 7369
_gp. 1075-9
856 4 0 _uhttps://doi.org/10.1016/s0140-6736(64)92605-4
_zAvailable from publisher's website
999 _c13969827
_d13969827