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Errata and notes of caution
Medwave 2019;19(5):e7657 doi: 10.5867/medwave.2019.05.7657
Correction to: Congenital myasthenic syndrome due to rapsyn deficiency: A case report with a new mutation and compound heterozygosity
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Correction to: 
Espinoza IO, Reynoso C, Chávez G, Engel AG. Congenital myasthenic syndrome due to rapsyn deficiency: A case report with a new mutation and compound heterozygosity. Medwave 2019;19(5):e7645 doi: 10.5867/medwave.2019.05.7645

18/06/2019

Corrected:
Funding notes Spanish HTML version:
The authors state that there were no external sources of funding for the preparation of this report.

For the following:
Dr. Engel's laboratory work was funded by NIH NS6277 of the National Institutes of Health of the United States of America. The rest of the authors state that there were no external sources of funding for the preparation of this report.

18/06/2019: The same change was made to the Spanish PDF version of the article. 

Licencia Creative Commons Esta obra de Medwave está bajo una licencia Creative Commons Atribución-NoComercial 3.0 Unported. Esta licencia permite el uso, distribución y reproducción del artículo en cualquier medio, siempre y cuando se otorgue el crédito correspondiente al autor del artículo y al medio en que se publica, en este caso, Medwave.

 


Citation: Editors. Correction to: Congenital myasthenic syndrome due to rapsyn deficiency: A case report with a new mutation and compound heterozygosity. Medwave 2019;19(5):e7657 doi: 10.5867/medwave.2019.05.7657

Publication date: 18/6/2019

PubMed record

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