Correction: Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome

Affiliations

¹ Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
² Children's Hospital of Eastern Ontario Research Institute; Division of Neurology, Department of Medicine, The Ottawa Hospital; Brain and Mind Research Institute, University of Ottawa, Ottawa, ON, Canada.
³ Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
⁴ Department of Human Genetics, National Institute of Mental Health and Neurosciences, Bengaluru, India.
⁵ Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
⁶ Department of Neuromuscular Research, National Institute of Neuroscience, Tokyo, Japan.
⁷ Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India. atchayaramnalini@yahoo.co.in.

^# Contributed equally.

Published Erratum

Mainak Bardhan et al. J Hum Genet. 2021 Aug.

. 2021 Aug;66(8):841.

doi: 10.1038/s10038-021-00920-2.

¹ Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
² Children's Hospital of Eastern Ontario Research Institute; Division of Neurology, Department of Medicine, The Ottawa Hospital; Brain and Mind Research Institute, University of Ottawa, Ottawa, ON, Canada.
³ Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
⁴ Department of Human Genetics, National Institute of Mental Health and Neurosciences, Bengaluru, India.
⁵ Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
⁶ Department of Neuromuscular Research, National Institute of Neuroscience, Tokyo, Japan.
⁷ Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India. atchayaramnalini@yahoo.co.in.

^# Contributed equally.

No abstract available

Erratum for

Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome.
Bardhan M, Polavarapu K, Bevinahalli NN, Veeramani PK, Anjanappa RM, Arunachal G, Shingavi L, Vengalil S, Nashi S, Chawla T, Nagabushana D, Mohan D, Horvath R, Nishino I, Atchayaram N. Bardhan M, et al. J Hum Genet. 2021 Aug;66(8):813-823. doi: 10.1038/s10038-021-00913-1. Epub 2021 Mar 12. J Hum Genet. 2021. PMID: 33712684