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The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 2006, Volume 117, Issue 4, pp. 725 - 738
The Wiskott-Aldrich syndrome (WAS) is a rare X-linked disorder with variable clinical phenotypes that correlate with the type of mutations in the ( ) gene.... 
Wiskott-Aldrich syndrome | X-linked thrombocytopenia | function of WASP | X-linked neutropenia | immune defects | mutation analysis | genotype-phenotype correlation | mutational hotspots | hematopoietic stem cell transplantation | gene therapy | scoring system | ACTIN POLYMERIZATION | IN-VIVO REVERSION | SYNDROME PROTEIN WASP | MEDIATED GENE-TRANSFER | ARP2/3 COMPLEX | T-CELL | IMMUNOLOGY | NK CELL CYTOTOXICITY | HEMATOPOIETIC-CELLS | ALLERGY | EPIDERMAL-GROWTH-FACTOR | Wiskott-Aldrich Syndrome Protein - genetics | Wiskott-Aldrich Syndrome - immunology | Neoplasms - etiology | Signal Transduction | Thrombocytopenia - etiology | Humans | Actins - metabolism | Cell Communication | Genotype | Male | Autoimmune Diseases - etiology | Wiskott-Aldrich Syndrome - genetics | Eczema - etiology | Thrombocytopenia - blood | Wiskott-Aldrich Syndrome - physiopathology | Phenotype | Models, Biological | Wiskott-Aldrich Syndrome Protein - metabolism | Mutation | Wiskott-Aldrich Syndrome - complications | Cell Movement | Medical colleges | Immunoglobulins | Genetic disorders | Dendritic cells | Children's hospitals | Guanosine | Polymerization | Transplantation | Muscle proteins | Hematopoietic stem cells | Phosphatidylinositol | Actin | Analysis | Children | Health aspects | Motility | Ear diseases | Gene expression | Patients | Cell adhesion & migration | Defects | Proteins | Genotype & phenotype | Genetic counseling | Lymphocytes | Eczema | Binding sites | Immune system
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