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Publications by Shepherd H. Schurman
Second-Site Mutation in the Wiskott-Aldrich Syndrome (WAS) Protein Gene Causes Somatic Mosaicism in Two WAS Siblings
Journal of Clinical Investigation
Medicine
Related publications
A Novel Splice Site Mutation in WAS Gene in Patient With Wiskott-Aldrich Syndrome and Chronic Colitis: A Case Report
BMC Medical Genetics
Genetics
A Novel Site Mutation in a Wiskott-Aldrich Syndrome Boy: A Case Report
Biomedical Journal of Scientific & Technical Research
Wiskott-Aldrich Syndrome
Wiskott-Aldrich Syndrome
Large Granular Lymphocyte Proliferation and Revertant Mosaicism: Two Rare Events in a Wiskott-Aldrich Syndrome Patient
Haematologica
Hematology
The Phenomenon of Reverse Mutation in a Patient With Wiskott–Aldrich Syndrome
Pediatric Hematology/Oncology and Immunopathology
Oncology
Pediatrics
Child Health
Allergy
Hematology
Perinatology
Immunology
When WAS Gene Diagnosis Is Needed: Seeking Clues Through Comparison Between Patients With Wiskott-Aldrich Syndrome and Idiopathic Thrombocytopenic Purpura
Frontiers in Immunology
Allergy
Immunology
Lessons From the Wiskott–Aldrich Syndrome
New England Journal of Medicine
Medicine
A Hydrophobic Pocket in the Active Site of Glycolytic Aldolase Mediates Interactions With Wiskott-Aldrich Syndrome Protein
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
