000 01390 a2200421 4500
005 20250515044340.0
264 0 _c20061101
008 200611s 0 0 eng d
022 _a1533-4406
024 7 _a10.1056/NEJMoa062520
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBinder, Vera
245 0 0 _aThe genotype of the original Wiskott phenotype.
_h[electronic resource]
260 _bThe New England journal of medicine
_cOct 2006
300 _a1790-3 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAmino Acid Sequence
650 0 4 _aBase Sequence
650 0 4 _aDNA Mutational Analysis
650 0 4 _aFemale
650 0 4 _aFrameshift Mutation
650 0 4 _aGenotype
650 0 4 _aHematopoietic Stem Cell Transplantation
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aPedigree
650 0 4 _aRNA, Messenger
_xanalysis
650 0 4 _aWiskott-Aldrich Syndrome
_xgenetics
650 0 4 _aWiskott-Aldrich Syndrome Protein
_xgenetics
700 1 _aAlbert, Michael H
700 1 _aKabus, Maria
700 1 _aBertone, Marko
700 1 _aMeindl, Alfons
700 1 _aBelohradsky, Bernd H
773 0 _tThe New England journal of medicine
_gvol. 355
_gno. 17
_gp. 1790-3
856 4 0 _uhttps://doi.org/10.1056/NEJMoa062520
_zAvailable from publisher's website
999 _c16640316
_d16640316