Erratum to ‘Cap myopathy caused by a mutation of the skeletal alpha-actin gene ACTA1’ [Neuromuscular Disorders 20 (2010) 238–240]

Hung, Ryan M.; Yoon, Grace; Hawkins, Cynthia E.; Halliday, Willliam; Biggar, Doug; Vajsar, Jiri

doi:10.1016/j.nmd.2010.06.015

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Volume 20, Issue 8 , Page 567, August 2010

Erratum to ‘Cap myopathy caused by a mutation of the skeletal alpha-actin gene ACTA1’ [Neuromuscular Disorders 20 (2010) 238–240]

Ryan M. Hung
- Division of Neurology, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada
- Pediatrics, Bloorviews Kids Rehab, Toronto, Ontario, Canada
Grace Yoon
- Division of Neurology, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada
- Divisions of Clinical/Metabolic Genetics, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada
Cynthia E. Hawkins
- Department of Pathology, The Hospital for Sick Children, Toronto, Ontario, Canada
Willliam Halliday
- Department of Pathology, The Hospital for Sick Children, Toronto, Ontario, Canada
Doug Biggar
- Pediatrics, Bloorviews Kids Rehab, Toronto, Ontario, Canada
Jiri Vajsar
- Division of Neurology, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada
- Corresponding author. Address: The Hospital for Sick Children, Toronto, Ontario, Canada M5G 1X8. Tel.: +1 416 813 5668; fax: +1 416 813 6334.

Article Outline

In the above published article the authors stated that the mutation in the alpha-actin gene ACTA1 was p.Met47Val. The correct mutation is p.Met49Val. The authors regret the error and apologize to the readers, editor and publishers.

PII: S0960-8966(10)00269-5

doi:10.1016/j.nmd.2010.06.015

Refers to article:

Cap myopathy caused by a mutation of the skeletal alpha-actin gene ACTA1
Ryan M. Hung, Grace Yoon, Cynthia E. Hawkins, Willliam Halliday, Doug Biggar, Jiri Vajsar
Neuromuscular Disorders April 2010 (Vol. 20, Issue 4, Pages 238-240)