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Quest Diagnostics

Non-coding and Mitochondrial DNA Variants Are Disease Causing for 1 in 20 Patients With Monogenic Diabetes

Human Genetics Society of Australasia
45th Annual Scientific Meeting

HGSA, 2022

Perth, Australia, November 24 - 27, 2022

Poster presentation: Non-coding and mitochondrial DNA variants are disease causing for 1 in 20 patients with monogenic diabetes

Authors: Scocchia A, Gall K, Hathaway J, Zilliacus E, Sluyters A, Archie Taylor A, Huusko J, Bernal M, Känsäkoski J, von Nandelstadh P, Tommiska J, Saarinen I,  Rantanen M, Schleit J, Gentile M, Pertteli Salmenperä P, Paananen J, Myllykangas S, Koskenvuo J

Specialties: Cardiology, Endocrinology, Genetics

Disclaimer:  One or more of the authors of this publication were employed at the time by Blueprint Genetics, a subsidiary of Quest Diagnostics.

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