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Diseases caused by mutations in ORAI1 and STIM1
Rodrigo S. Lacruz
, Stefan Feske
Molecular Pathobiology
Research output
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peer-review
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Medicine & Life Sciences
ORAI1 Protein
99%
Gain of Function Mutation
97%
Stromal Interaction Molecule 1
79%
Loss of Function Mutation
55%
Mutation
55%
Muscular Diseases
53%
Stormorken Syndrome
52%
Congenital Structural Myopathies
38%
Ectodermal Dysplasia
34%
Channelopathies
34%
Sweat Glands
31%
Severe Combined Immunodeficiency
31%
Disease Susceptibility
27%
Dental Enamel
26%
Autoimmunity
24%
Endoplasmic Reticulum
23%
Thrombocytopenia
23%
Ions
20%
Skeletal Muscle
19%
Blood Platelets
19%
Homeostasis
18%
Cell Membrane
18%
Tooth
17%
Hemorrhage
15%
Genes
9%
Arts & Humanities
Mutation
100%
Syndrome
65%
Protein
59%
Defects
48%
Homeostasis
37%
Autoimmunity
36%
Diathesis
35%
Plasma
33%
Enamel
31%
Activation
26%
Teeth
25%
Conducting
24%
Molecules
23%
Physiology
22%
Membrane
22%
Gene
21%
Cells
17%
Causes
14%
Interaction
13%
Chemical Compounds
Mutation
83%
Protein
20%
Pore
16%
Plasma
15%