Genotype-phenotype correlation in Bruton's tyrosine kinase deficiency.

Teimourian, Shahram; Nasseri, Saeed; Pouladi, Nima; Yeganeh, Mehdi; Aghamohammadi, Asghar

Teimourian, Shahram; Nasseri, Saeed; Pouladi, Nima; Yeganeh, Mehdi; Aghamohammadi, Asghar.

Affiliation

Teimourian S; Immunology, Asthma and Allergy Research Institute, Tehran University of Medical Sciences, Tehran, Iran. teimourian@tums.ac.ir

J Pediatr Hematol Oncol ; 30(9): 679-83, 2008 Sep.

Article in En | MEDLINE | ID: mdl-18776760

Subject(s)

Agammaglobulinemia/genetics; Protein-Tyrosine Kinases/deficiency; Agammaglobulinaemia Tyrosine Kinase; Agammaglobulinemia/pathology; Cohort Studies; DNA Mutational Analysis; Family Health; Genetic Diseases, X-Linked; Genotype; Humans; Mutation; Phenotype; Protein-Tyrosine Kinases/genetics; Severity of Illness Index

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protein-Tyrosine Kinases / Agammaglobulinemia Type of study: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Humans Language: En Journal: J Pediatr Hematol Oncol Journal subject: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Year: 2008 Type: Article Affiliation country: Iran

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