| 000 | 01609 a2200493 4500 | ||
|---|---|---|---|
| 005 | 20250511201201.0 | ||
| 264 | 0 | _c19901121 | |
| 008 | 199011s 0 0 eng d | ||
| 022 | _a0028-4793 | ||
| 024 | 7 |
_a10.1056/NEJM199010253231707 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aYamashina, M | |
| 245 | 0 | 0 |
_aInherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria. _h[electronic resource] |
| 260 |
_bThe New England journal of medicine _cOct 1990 |
||
| 300 |
_a1184-9 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAcetylcholinesterase _xanalysis |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aBlood Proteins _xanalysis |
| 650 | 0 | 4 | _aCD55 Antigens |
| 650 | 0 | 4 | _aCD59 Antigens |
| 650 | 0 | 4 |
_aCarrier Proteins _xanalysis |
| 650 | 0 | 4 | _aCell Separation |
| 650 | 0 | 4 | _aCells, Cultured |
| 650 | 0 | 4 |
_aErythrocyte Membrane _xchemistry |
| 650 | 0 | 4 |
_aFibroblasts _xchemistry |
| 650 | 0 | 4 | _aFlow Cytometry |
| 650 | 0 | 4 |
_aHemoglobinuria, Paroxysmal _xblood |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aImmunohistochemistry |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMembrane Proteins _xanalysis |
| 700 | 1 | _aUeda, E | |
| 700 | 1 | _aKinoshita, T | |
| 700 | 1 | _aTakami, T | |
| 700 | 1 | _aOjima, A | |
| 700 | 1 | _aOno, H | |
| 700 | 1 | _aTanaka, H | |
| 700 | 1 | _aKondo, N | |
| 700 | 1 | _aOrii, T | |
| 700 | 1 | _aOkada, N | |
| 773 | 0 |
_tThe New England journal of medicine _gvol. 323 _gno. 17 _gp. 1184-9 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1056/NEJM199010253231707 _zAvailable from publisher's website |
| 999 |
_c1705525 _d1705525 |
||