000			01801 a2200577 4500
005			20250511234141.0
264		0	_c19900525
008			199005s 0 0 eng d
022			_a0006-4971
040			_aNLM _beng _cNLM
100	1		_aGarbarz, M
245	0	0	_aHereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain. _h[electronic resource]
260			_bBlood _cApr 1990
300			_a1691-8 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650	0	4	_aAdult
650	0	4	_aAged
650	0	4	_aAlleles
650	0	4	_aAmino Acid Sequence
650	0	4	_aAnemia, Hemolytic, Congenital _xgenetics
650	0	4	_aBase Sequence
650	0	4	_aCodon _xgenetics
650	0	4	_aDNA _xanalysis
650	0	4	_aElliptocytosis, Hereditary _xgenetics
650	0	4	_aErythrocyte Count
650	0	4	_aErythrocyte Deformability
650	0	4	_aErythrocyte Membrane _xanalysis
650	0	4	_aFemale
650	0	4	_aGenetic Variation
650	0	4	_aHumans
650	0	4	_aMale
650	0	4	_aMembrane Proteins _xanalysis
650	0	4	_aMiddle Aged
650	0	4	_aMolecular Sequence Data
650	0	4	_aOligonucleotides _xgenetics
650	0	4	_aPedigree
650	0	4	_aPolymerase Chain Reaction
650	0	4	_aRNA, Messenger _xgenetics
650	0	4	_aSpectrin _xgenetics
650	0	4	_aTrypsin _xpharmacology
700	1		_aLecomte, M C
700	1		_aFéo, C
700	1		_aDevaux, I
700	1		_aPicat, C
700	1		_aLefebvre, C
700	1		_aGalibert, F
700	1		_aGautero, H
700	1		_aBournier, O
700	1		_aGaland, C
773	0		_tBlood _gvol. 75 _gno. 8 _gp. 1691-8
999			_c2334397 _d2334397