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X-Linked Agammaglobulinemia clinical trials

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NCT ID: NCT00004341 Active, not recruiting - Clinical trials for Wiskott-Aldrich Syndrome

Study of Genetic and Molecular Defects in Primary Immunodeficiency Disorders

Start date: July 1995
Phase: N/A
Study type: Observational

OBJECTIVES: I. Identify the molecular defects responsible for primary immunodeficiency disorders. II. Explore the mutations within each syndrome to better understand the genetics of these disorders. III. Study the function of the Wiskott-Aldrich syndrome proteins (WASP). IV. Design methods to identify carriers and for prenatal diagnosis. V. Explore new avenues for therapy.