Feature Story: University of Regina research team makes significant discovery into a rare disease

dc.contributor.authorUniversity Advancement & Communications, University of Regina
dc.date.accessioned2022-04-26T17:26:24Z
dc.date.available2022-04-26T17:26:24Z
dc.date.issued2019-10-01
dc.description.abstractAccording to the World Health Organization rare diseases are often serious, chronic, and life threatening. In Canada, about one in twelve people are affected by a rare disease. Most are caused by gene mutations, including those in mitochondria, which are what generate energy in our cells to keep our bodies functioning. And a mutation in the mitochondrial gene can contribute to rare disorders.en_US
dc.description.authorstatusStaffen_US
dc.description.peerreviewnoen_US
dc.identifier.urihttps://hdl.handle.net/10294/14732
dc.language.isoenen_US
dc.publisherUniversity Advancement & Communications, University of Reginaen_US
dc.subjectWorld Health Organizationen_US
dc.subjectiScineceen_US
dc.subjectDepartment of Biochemistryen_US
dc.subjectCanadian Organization for Rare Disordersen_US
dc.subjectCRISPRen_US
dc.titleFeature Story: University of Regina research team makes significant discovery into a rare diseaseen_US
dc.typeOtheren_US
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