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. 2022 Dec 22;32(7):1236. doi: 10.1093/hmg/ddac294

Correction to: Deleterious variants in CRLS1 lead to cardiolipin deficiency and cause an autosomal recessive multi-system mitochondrial disease

PMCID: PMC10026221  PMID: 36563328

This is a correction to: Richard G Lee, Shanti Balasubramaniam, Maike Stentenbach, Tom Kralj, Tim McCubbin, Benjamin Padman, Janine Smith, Lisa G Riley, Archana Priyadarshi, Liuyu Peng, Madison R Nuske, Richard Webster, Ken Peacock, Philip Roberts, Zornitza Stark, Gabrielle Lemire, Yoko A Ito, Care4Rare Canada Consortium, Kym M Boycott, Michael T Geraghty, Jan Bert van Klinken, Sacha Ferdinandusse, Ying Zhu, Rebecca Walsh, Esteban Marcellin, David R Thorburn, Tony Roscioli, Janice Fletcher, Oliver Rackham, Frédéric M Vaz, Gavin E Reid, Aleksandra Filipovska, Deleterious variants in CRLS1 lead to cardiolipin deficiency and cause an autosomal recessive multi-system mitochondrial disease, Human Molecular Genetics, Volume 31, Issue 21, 1 November 2022, Pages 3597–3612, https://doi.org/10.1093/hmg/ddac040

In the originally published version of this manuscript, the names of authors Tony Roscioli and Ying Zhu were inadvertently misspelled.

These errors have been corrected online.


Articles from Human Molecular Genetics are provided here courtesy of Oxford University Press

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