000 01273 a2200349 4500
005 20250511141738.0
264 0 _c19780218
008 197802s 0 0 eng d
022 _a0009-8981
024 7 _a10.1016/0009-8981(77)90007-9
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMarie, J
245 0 0 _aHereditary erythrocyte pyruvate kinase deficiency: molecular and functional studies of four mutant PK variants detected in Spain.
_h[electronic resource]
260 _bClinica chimica acta; international journal of clinical chemistry
_cDec 1977
300 _a153-62 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAntigens
_xanalysis
650 0 4 _aBlood Protein Electrophoresis
650 0 4 _aComplement Fixation Tests
650 0 4 _aErythrocytes
_xenzymology
650 0 4 _aHumans
650 0 4 _aIsoelectric Focusing
650 0 4 _aKinetics
650 0 4 _aMutation
650 0 4 _aPyruvate Kinase
_xdeficiency
650 0 4 _aSpain
700 1 _aVives-Corrons, J L
700 1 _aKahn, A
700 1 _aKernemp, B
773 0 _tClinica chimica acta; international journal of clinical chemistry
_gvol. 81
_gno. 2
_gp. 153-62
856 4 0 _uhttps://doi.org/10.1016/0009-8981(77)90007-9
_zAvailable from publisher's website
999 _c610158
_d610158