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Annals of Clinical and Translational Neurology logoLink to Annals of Clinical and Translational Neurology
. 2017 May 8;4(5):356. doi: 10.1002/acn3.422

Corrigendum

PMCID: PMC5420802  PMID: 28491904

Novel synaptobrevin‐1 mutation causes fatal congenital myasthenic syndrome. Volume 4. Issue 2, pp 130 and pp 133.

https://doi.org/10.1002/acn3.387

Errors were identified in the Abstract (pp 130) and in the Mutation analysis section (pp 133) of the published article.

The mutation in isoform D of SYB1‐ p.Ser114ValfsTer32 should be pSer114ValfsTer34. The mutation elongates the intravesicular C‐terminus of the D isoform from 4 to 33 residues rather than from 4 to 31 residues.

In the Abstract, the sentence should read, “The identified mutation elongates the intravesicular C‐terminus of the A isoform from 5 to 71, and of the D isoform from 4 to 33 residues.”

The authors apologize for this error.


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