作者：
Alexandra,Roston [1]
;
Dan,Evans [2]
;
Harinder,Gill [3]
;
Margaret,McKinnon [4]
;
Bertrand,Isidor [3]
;
Benjamin,Cogné [5]
;
Jill,Mwenifumbo [5]
;
Clara,van Karnebeek [6]
;
Jianghong,An [3]
;
Steven J M,Jones [7]
;
Matthew,Farrer [8]
;
Michelle,Demos [9]
;
Mary,Connolly [10]
;
William T,Gibson [10]
;
CAUSES Study [2]
;
EPGEN Study [11]
作者单位：
Department of Medical Genetics, The University of British Columbia, Vancouver, British Columbia, Canada alexandra.roston@phsa.ca.
[1]
Centre for Applied Neurogenetics, The University of British Columbia, Vancouver, British Columbia, Canada.
[2]
Department of Medical Genetics, The University of British Columbia, Vancouver, British Columbia, Canada.
[3]
Provincial Medical Genetics Program, BC Women's Hospital and Health Centre, Vancouver, British Columbia, Canada.
[4]
Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, Pays de la Loire, France.
[5]
INSERM, CNRS, UNIV Nantes, l'institut du thorax, Nantes, Frances.
[6]
Centre for Molecular Medicine and Therapeutics, University of British Columbia, Vancouver, British Columbia, Canada.
[7]
Department of Pediatrics, Emma Children's Hospital, Amsterdam Gastroenterology and Metabolism, Amsterdam University Medical Centres, University of Amsterdam, Amsterdam, Netherlands.
[8]
Department of Pediatrics, Radboud Centre for Mitochondrial Medicine, Radboud University Medical Centre, Nijmegen, Netherlands.
[9]
Canada's Michael Smith Genome Sciences Centre, Vancouver, British Columbia, Canada.
[10]
Division of Neurology, Department of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada.
[11]
DOI
10.1136/jmedgenet-2019-106756
PMID
32546566
发布时间
2022-12-07
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