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A Middle Eastern Founder Mutation Expands the Genotypic and Phenotypic Spectrum of Mitochondrial MICU1 Deficiency: A Report of 13 Patients.
scientific article published on 3 May 2018
Author/s
author: Tawfeg Ben-Omran, Vamsi Mootha, Jane Juusola
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Publication date
May 3, 2018
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