Response to correspondence of NDUFS4-related Leigh syndrome in Hutterites.

Lamont, Ryan E; Beaulieu, Chandree L; Bernier, Francois P; Sparkes, Rebecca; Innes, A Micheil; Jackel-Cram, Candice; Ober, Carole; Parboosingh, Jillian S; Lemire, Edmond G

Lamont, Ryan E; Beaulieu, Chandree L; Bernier, Francois P; Sparkes, Rebecca; Innes, A Micheil; Jackel-Cram, Candice; Ober, Carole; Parboosingh, Jillian S; Lemire, Edmond G.

Affiliation

Lamont RE; Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Alberta.
Beaulieu CL; Alberta Children's Hospital Research Institute, University of Calgary, Calgary, Alberta.
Bernier FP; Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Alberta.
Sparkes R; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario.
Innes AM; Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Alberta.
Jackel-Cram C; Alberta Children's Hospital Research Institute, University of Calgary, Calgary, Alberta.
Ober C; Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Alberta.
Parboosingh JS; Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Alberta.
Lemire EG; Alberta Children's Hospital Research Institute, University of Calgary, Calgary, Alberta.

Am J Med Genet A ; 173(5): 1452, 2017 May.

Article in En | MEDLINE | ID: mdl-28371264

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Leigh Disease / Genetic Association Studies / Mutation / NADH Dehydrogenase Type of study: Prognostic_studies Limits: Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2017 Document type: Article Country of publication: Estados Unidos

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