Fe de erratas y notas de reserva
← vista completaPublicado el 18 de junio de 2019 | http://doi.org/10.5867/medwave.2019.05.7654
Correccion a: Síndrome miasténico congénito por deficiencia de rapsina: reporte de caso con nueva mutación y heterocigosidad compuesta
Correction to: Congenital myasthenic syndrome due to rapsyn deficiency: A case report with a new mutation and compound heterozygosity
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.
