Primary immunodeficiency diseases due to defects in lymphocytes.

[91] Atypical X-linked severe combined immunodeficiency due to possible spontaneous reversion of the genetic defect in T cells [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (21) : 1563 - 1567

[92] The interleukin-2 receptor gamma chain: Its role in the multiple cytokine receptor complexes and T cell development in XSCID [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 : 179 - 205

[93] Sullivan J L, 1989, Immunodefic Rev, V1, P325

[94] Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization [J]. CELL, 1996, 84 (05) : 723 - 734

[95] Leukemia and lymphoma in ataxia telangiectasia [J]. BLOOD, 1996, 87 (02) : 423 - 438

[96] A case of primary immunodeficiency due to a defect of the major histocompatibility gene complex class I processing and presentation pathway [J]. IMMUNOLOGY LETTERS, 1997, 57 (1-3) : 183 - 187

[97] DEFICIENT EXPRESSION OF A B-CELL CYTOPLASMIC TYROSINE KINASE IN HUMAN X-LINKED AGAMMAGLOBULINEMIA [J]. CELL, 1993, 72 (02) : 279 - 290

[98] THE GENE INVOLVED IN X-LINKED AGAMMAGLOBULINEMIA IS A MEMBER OF THE SRC FAMILY OF PROTEIN-TYROSINE KINASES (VOL 361, PG 226, 1993) [J]. NATURE, 1993, 364 (6435) : 362 - 362

[99] BTKbase, mutation database for X-linked agammaglobulinemia (XLA) [J]. NUCLEIC ACIDS RESEARCH, 1998, 26 (01) : 242 - 247

[100] X-LINKED THROMBOCYTOPENIA AND WISKOTT-ALDRICH SYNDROME ARE ALLELIC DISEASES WITH MUTATIONS IN THE WASP GENE [J]. NATURE GENETICS, 1995, 9 (04) : 414 - 417

[91] Atypical X-linked severe combined immunodeficiency due to possible spontaneous reversion of the genetic defect in T cells [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (21) : 1563 - 1567

[92] The interleukin-2 receptor gamma chain: Its role in the multiple cytokine receptor complexes and T cell development in XSCID [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 : 179 - 205

[93] Sullivan J L, 1989, Immunodefic Rev, V1, P325

[94] Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization [J]. CELL, 1996, 84 (05) : 723 - 734

[95] Leukemia and lymphoma in ataxia telangiectasia [J]. BLOOD, 1996, 87 (02) : 423 - 438

[96] A case of primary immunodeficiency due to a defect of the major histocompatibility gene complex class I processing and presentation pathway [J]. IMMUNOLOGY LETTERS, 1997, 57 (1-3) : 183 - 187

[97] DEFICIENT EXPRESSION OF A B-CELL CYTOPLASMIC TYROSINE KINASE IN HUMAN X-LINKED AGAMMAGLOBULINEMIA [J]. CELL, 1993, 72 (02) : 279 - 290

[98] THE GENE INVOLVED IN X-LINKED AGAMMAGLOBULINEMIA IS A MEMBER OF THE SRC FAMILY OF PROTEIN-TYROSINE KINASES (VOL 361, PG 226, 1993) [J]. NATURE, 1993, 364 (6435) : 362 - 362

[99] BTKbase, mutation database for X-linked agammaglobulinemia (XLA) [J]. NUCLEIC ACIDS RESEARCH, 1998, 26 (01) : 242 - 247

[100] X-LINKED THROMBOCYTOPENIA AND WISKOTT-ALDRICH SYNDROME ARE ALLELIC DISEASES WITH MUTATIONS IN THE WASP GENE [J]. NATURE GENETICS, 1995, 9 (04) : 414 - 417