Bi-allelic MCM10 variants associated with immune dysfunction and cardiomyopathy cause telomere shortening

Minichromosome maintenance protein 10 (MCM10) is essential for eukaryotic DNA replication. Here, we describe compound heterozygous MCM10 variants in patients with distinctive, but overlapping, clinical phenotypes: natural killer (NK) cell deficiency (NKD) and restrictive cardiomyopathy (RCM) with hy...

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Detalles Bibliográficos
Autores principales: Baxley, Ryan M., Leung, Wendy, Schmit, Megan M., Matson, Jacob Peter, Yin, Lulu, Oram, Marissa K., Wang, Liangjun, Taylor, John, Hedberg, Jack, Rogers, Colette B., Harvey, Adam J., Basu, Debashree, Taylor, Jenny C., Pagnamenta, Alistair T., Dreau, Helene, Craft, Jude, Ormondroyd, Elizabeth, Watkins, Hugh, Hendrickson, Eric A., Mace, Emily M., Orange, Jordan S., Aihara, Hideki, Stewart, Grant S., Blair, Edward, Cook, Jeanette Gowen, Bielinsky, Anja-Katrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7955084/
https://www.ncbi.nlm.nih.gov/pubmed/33712616
http://dx.doi.org/10.1038/s41467-021-21878-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7955084/
https://www.ncbi.nlm.nih.gov/pubmed/33712616
http://dx.doi.org/10.1038/s41467-021-21878-x

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