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HARVARD Citation
Salvi, A. et al. (2021). A novel bi‐allelic loss‐of‐function mutation in STIM1 expands the phenotype of STIM1‐related diseases. Clinical genetics. 100 (1), pp. 84-89. [Online].
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Salvi, A. et al. (2021). A novel bi‐allelic loss‐of‐function mutation in STIM1 expands the phenotype of STIM1‐related diseases. Clinical genetics. 100 (1), pp. 84-89. [Online].