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Unique mutations of Bruton's tyrosine kinase in fourteen unrelated X-linked agammaglobulinemia families
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1994
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Qili Zhu DepartmentGeneticsImmunodeficienciesTyrosine KinaseUnique MutationsPathologyMolecular GeneticsDisease Gene IdentificationGenetic MedicineClinical GeneticsMendelian DisorderReceptor Tyrosine KinaseMolecular OncologyInherited Metabolic DiseaseInborn Error Of ImmunityMolecular MedicineMolecular Diagnostic TechniquesSomatic VariantGenetic DisorderMedical GeneticsMedicineUsa SearchLysosomal Storage Disease
Journal Article Unique mutations of Bruton's tyrosine kinase in fourteen unrelated X-linked agammaglobulinemia families Get access Qili Zhu, Qili Zhu Department of Pediatrics, University of Washington School of MedicineSeattle WA 98195 Search for other works by this author on: Oxford Academic PubMed Google Scholar Min Zhang, Min Zhang Department of Pediatrics, University of Washington School of MedicineSeattle WA 98195 Search for other works by this author on: Oxford Academic PubMed Google Scholar Jerry Winkelstein, Jerry Winkelstein 1Department of Pediatrics, Johns Hopkins University School of MedicineBaltimore, MD 21205, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar Shi-Han Chen, Shi-Han Chen Department of Pediatrics, University of Washington School of MedicineSeattle WA 98195 Search for other works by this author on: Oxford Academic PubMed Google Scholar Hans D. Ochs Hans D. Ochs * Department of Pediatrics, University of Washington School of MedicineSeattle WA 98195 * To whom correspondence should be addressed Search for other works by this author on: Oxford Academic PubMed Google Scholar Human Molecular Genetics, Volume 3, Issue 10, October 1994, Pages 1899–1900, https://doi.org/10.1093/hmg/3.10.1899 Published: 01 October 1994 Article history Received: 15 June 1994 Revision received: 05 August 1994 Accepted: 05 August 1994 Published: 01 October 1994