Whole exome sequencing analysis of 1000 Latin American patients affected by a neuromuscular disorder. Preliminary data

Authors

  • ANDREA NOVAS MALDONADO INSTITUTO NACIONAL DE REHABILITACION
  • Alexandra Luna Angulo Medicina Genómica, Instituto Nacional de Rehabilitación, MEXICO
  • Rosa Elena Escobar Cedillo Rehabilitación, Instituto Nacional de Rehabilitación, MEXICO
  • Ana Topf John Walton Muscular Dystrophy Research Centre, Institute of Translational and Clinical Research University of Newcastle, REINO UNIDO DE LA GRAN BRETAÑA E IRLANDA DEL NORTE
  • Alejandro Gonzalez Chamorro John Walton Muscular Dystrophy Research Centre, Institute of Translational and Clinical Research University of Newcastle, REINO UNIDO DE LA GRAN BRETAÑA E IRLANDA DEL NORTE
  • Jordi Díaz Manera John Walton Muscular Dystrophy Research Centre, Institute of Translational and Clinical Research University of Newcastle, ESPAÑA
  • Antonio Miranda Duarte Medicina Genómica, Instituto Nacional de Rehabilitación, MEXICO

Keywords:

WHOLE EXOME, NEUROMUSCULAR DISEASE, MOLECULAR DIAGNOSIS

References

No aplica

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Published

2024-10-11

How to Cite

1.
NOVAS MALDONADO A, Luna Angulo A, Escobar Cedillo RE, Topf A, Gonzalez Chamorro A, Díaz Manera J, et al. Whole exome sequencing analysis of 1000 Latin American patients affected by a neuromuscular disorder. Preliminary data. InDiscap [Internet]. 2024 Oct. 11 [cited 2024 Oct. 18];10(S1). Available from: https://dsm.inr.gob.mx/indiscap/index.php/INDISCAP/article/view/142

Issue

Vol. 10 No. S1 (2024): Abstracts from the International Congress of Rehabilitation Research 2024

Section

CIIR - Investigación clínica

License

Copyright (c) 2024 Instituto Nacional de Rehabilitación Luis Guillermo Ibarra Ibarra

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

© Instituto Nacional de Rehabilitación Luis Guillermo Ibarra Ibarra under a Creative Commons Attribution 4.0 International (CC BY 4.0) license which allows to reproduce and modify the content if appropiate recognition to the original source is given.

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