Robust Preimplantation Genetic Testing Strategy for Myotonic Dystrophy Type 1 by Bidirectional Triplet-Primed Polymerase Chain Reaction Combined With Multi-microsatellite Haplotyping Following Whole-Genome Amplification

Myotonic dystrophy type 1 (DM1) is caused by expansion of the DMPK CTG trinucleotide repeat. Disease transmission to offspring can be avoided through prenatal diagnosis or preimplantation genetic testing for monogenic disorders (PGT-M). We describe a robust strategy for DM1 PGT-M that can be applied...

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Detalles Bibliográficos
Autores principales: Lian, Mulias, Lee, Caroline G., Chong, Samuel S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611416/
https://www.ncbi.nlm.nih.gov/pubmed/31316546
http://dx.doi.org/10.3389/fgene.2019.00589

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611416/
https://www.ncbi.nlm.nih.gov/pubmed/31316546
http://dx.doi.org/10.3389/fgene.2019.00589

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