Reply: ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability

Timothy J Edwards^{1

2}, Elliott H Sherr³, A James Barkovich⁴, Linda J Richards^{1

5}

Affiliations

¹ The University of Queensland, Queensland Brain Institute, Brisbane, 4072, Australia.
² The University of Queensland, School of Medicine, Brisbane, 4072, Australia.
³ Departments of Neurology and Paediatrics, The University of California and the Benioff Children's Hospital, CA, 94158, USA.
⁴ UCSF Medical Center and Benioff Children's Hospital, San Francisco, CA, 94143, USA.
⁵ The University of Queensland, School of Biomedical Sciences, Brisbane, 4072, Australia.

Comment

Timothy J Edwards et al. Brain. 2016.

. 2016 Nov 1;139(11):e65.

doi: 10.1093/brain/aww171.

Timothy J Edwards^{1

2}, Elliott H Sherr³, A James Barkovich⁴, Linda J Richards^{1

5}

¹ The University of Queensland, Queensland Brain Institute, Brisbane, 4072, Australia.
² The University of Queensland, School of Medicine, Brisbane, 4072, Australia.
³ Departments of Neurology and Paediatrics, The University of California and the Benioff Children's Hospital, CA, 94158, USA.
⁴ UCSF Medical Center and Benioff Children's Hospital, San Francisco, CA, 94143, USA.
⁵ The University of Queensland, School of Biomedical Sciences, Brisbane, 4072, Australia.

No abstract available

Comment on

Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes.
Edwards TJ, Sherr EH, Barkovich AJ, Richards LJ. Edwards TJ, et al. Brain. 2014 Jun;137(Pt 6):1579-613. doi: 10.1093/brain/awt358. Epub 2014 Jan 28. Brain. 2014. PMID: 24477430 Free PMC article. Review.
ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability.
Mignot C, Moutard ML, Rastetter A, Boutaud L, Heide S, Billette T, Doummar D, Garel C, Afenjar A, Jacquette A, Lacombe D, Verloes A, Bole-Feysot C, Nitschké P, Masson C, Faudet A, Lesne F, Bienvenu T, Alby C, Attié-Bitach T, Depienne C, Nava C, Héron D. Mignot C, et al. Brain. 2016 Nov 1;139(11):e64. doi: 10.1093/brain/aww181. Brain. 2016. PMID: 27474218 No abstract available.

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