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