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Publications by Erik Sandholm
Compound Heterozygous Mutations of IL2-Inducible T Cell Kinase in a Swedish Patient: The Importance of Early Genetic Diagnosis
Journal of Clinical Immunology
Allergy
Immunology
Related publications
Novel Compound Heterozygous Mutations in the Pantothenate Kinase 2 Gene in a Korean Patient With Atypical Pantothenate Kinase Associated Neurodegeneration
Journal of Movement Disorders
Early Onset Mandibuloacral Dysplasia Due to Compound Heterozygous Mutations in ZMPSTE24
American Journal of Medical Genetics, Part A
Genetics
SRC-Induced Activation of Inducible T Cell Kinase (ITK) Requires Phosphatidylinositol 3-Kinase Activity and the Pleckstrin Homology Domain of Inducible T Cell Kinase
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Inducible T Cell Kinase (ITK); IL-2
Science-Business eXchange
Importance of Early Diagnosis
Advances in Pulmonary Hypertension
Genetic Diagnosis of Familial Hypercholesterolaemia: The Importance of Functional Analysis of Potential Splice-Site Mutations
Journal of Medical Genetics
Genetics
Squamous Cell Thyroid Carcinoma, the Importance of Early Diagnosis and Treatment
Endocrine Abstracts
Compound Heterozygous Hemophilia a in a Female Patient and the Identification of a Novel Missense Mutation, p.Met1093Ile
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Congenital Dyserythropoietic Anemia Type 1: A Case With Novel Compound Heterozygous Mutations in the C15orf41 Gene
American Journal of Hematology
Hematology
