000 01392 a2200433 4500
005 20250511200412.0
264 0 _c19910725
008 199107s 0 0 eng d
022 _a0140-6736
024 7 _a10.1016/0140-6736(91)93263-9
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSumiya, M
245 0 0 _aMolecular basis of opsonic defect in immunodeficient children.
_h[electronic resource]
260 _bLancet (London, England)
_cJun 1991
300 _a1569-70 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAlleles
650 0 4 _aCarrier Proteins
_xblood
650 0 4 _aDNA
_xanalysis
650 0 4 _aExons
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aImmunologic Deficiency Syndromes
_xblood
650 0 4 _aInfant, Newborn
650 0 4 _aMannose-Binding Lectins
650 0 4 _aMolecular Sequence Data
650 0 4 _aMutation
_xgenetics
650 0 4 _aNucleic Acid Probes
650 0 4 _aOpsonin Proteins
_xgenetics
650 0 4 _aPedigree
700 1 _aSuper, M
700 1 _aTabona, P
700 1 _aLevinsky, R J
700 1 _aArai, T
700 1 _aTurner, M W
700 1 _aSummerfield, J A
773 0 _tLancet (London, England)
_gvol. 337
_gno. 8757
_gp. 1569-70
856 4 0 _uhttps://doi.org/10.1016/0140-6736(91)93263-9
_zAvailable from publisher's website
999 _c1682125
_d1682125