Stormorken Syndrome Caused by a Novel STIM1 Mutation: A Case Report
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DOI: 10.3389/fneur.2021.522513
Abstract: Objective: To identify the gene mutation of Stormorken syndrome and review the published Stromal Interaction Molecule 1 (STIM1) mutation phenotype. Methods: We described the clinical and molecular aspects of a Chinese female with Stormorken syndrome… read more here.
Keywords: novel stim1; syndrome caused; stormorken syndrome; caused novel ... See more keywords