Correction: Genome and RNA sequencing in patients with methylmalonic aciduria of unknown cause

Lina Sobhi Abdrabo¹, David Watkins^{1

2}, Sophie Ran Wang¹, Joël Lafond-Lapalme¹, Jean-Baptiste Riviere^{1

2}, David S Rosenblatt^{3

4

5}

Affiliations

¹ Department of Human Genetics, McGill University, Montreal, QC, Canada.
² Division of Medical Genetics, Department of Specialized Medicine, McGill University Health Centre, Montreal, QC, Canada.
³ Department of Human Genetics, McGill University, Montreal, QC, Canada. david.rosenblatt@mcgill.ca.
⁴ Division of Medical Genetics, Department of Specialized Medicine, McGill University Health Centre, Montreal, QC, Canada. david.rosenblatt@mcgill.ca.
⁵ Division of Medical Biochemistry, Department of Specialized Medicine, McGill University Health Centre, Montreal, QC, Canada. david.rosenblatt@mcgill.ca.

Free article

Published Erratum

Lina Sobhi Abdrabo et al. Genet Med. 2020 Jul.

Free article

. 2020 Jul;22(7):1280.

doi: 10.1038/s41436-020-0852-z.

Lina Sobhi Abdrabo¹, David Watkins^{1

2}, Sophie Ran Wang¹, Joël Lafond-Lapalme¹, Jean-Baptiste Riviere^{1

2}, David S Rosenblatt^{3

4

5}

¹ Department of Human Genetics, McGill University, Montreal, QC, Canada.
² Division of Medical Genetics, Department of Specialized Medicine, McGill University Health Centre, Montreal, QC, Canada.
³ Department of Human Genetics, McGill University, Montreal, QC, Canada. david.rosenblatt@mcgill.ca.
⁴ Division of Medical Genetics, Department of Specialized Medicine, McGill University Health Centre, Montreal, QC, Canada. david.rosenblatt@mcgill.ca.
⁵ Division of Medical Biochemistry, Department of Specialized Medicine, McGill University Health Centre, Montreal, QC, Canada. david.rosenblatt@mcgill.ca.

Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Genome and RNA sequencing in patients with methylmalonic aciduria of unknown cause.
Abdrabo LS, Watkins D, Wang SR, Lafond-Lapalme J, Riviere JB, Rosenblatt DS. Abdrabo LS, et al. Genet Med. 2020 Feb;22(2):432-436. doi: 10.1038/s41436-019-0640-9. Epub 2019 Aug 29. Genet Med. 2020. PMID: 31462756