Novel Homozygous Variant in COQ7 in Siblings With Hereditary Motor Neuropathy

Author:

Smith Ian C.1ORCID,Pileggi Chantal A.1ORCID,Wang Ying1ORCID,Kernohan Kristin1,Hartley Taila1ORCID,McMillan Hugh J.1ORCID,Sampaio Marcos Loreto1ORCID,Melkus Gerd1ORCID,Woulfe John1ORCID,Parmar Gaganvir1,Bourque Pierre R.1ORCID,Breiner Ari1ORCID,Zwicker Jocelyn1ORCID,Pringle C. Elizabeth1,Jarinova Olga1ORCID,Lochmüller Hanns1ORCID,Dyment David A.1ORCID,Brais Bernard1ORCID,Boycott Kym M.1ORCID,Hekimi Siegfried1ORCID,Harper Mary-Ellen1ORCID,Warman-Chardon Jodi1ORCID

Affiliation:

1. From the The Ottawa Hospital Research Institute (I.C.S., M.L.S., G.M., A.B., J.Z., H.L., J.W.-C.), Ottawa; Department of Biochemistry, Microbiology and Immunology (C.A.P., G.P., M.-E.H.), Faculty of Medicine, University of Ottawa, Ontario; Ottawa Institute of Systems Biology (C.A.P., G.P., M.-E.H.), University of Ottawa, Ontario; Department of Biology (Y.W., S.H.), McGill University, Montreal, Quebec; Children's Hospital of Eastern Ontario Research Institute (K.K., T.H., O.J., H.L., D.A.D., K.M.B.,...

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),Neurology (clinical)

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