Bi-allelic loss of function variants in SLC30A5 as cause of perinatal lethal cardiomyopathy

Perinatal mortality is a heavy burden for both affected parents and physicians. However, the underlying genetic causes have not been sufficiently investigated and most cases remain without diagnosis. This impedes appropriate counseling or therapy. We describe four affected children of two unrelated...

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Detalles Bibliográficos
Autores principales: Lieberwirth, Johann Kaspar, Joset, Pascal, Heinze, Anja, Hentschel, Julia, Stein, Anja, Iannaccone, Antonella, Steindl, Katharina, Kuechler, Alma, Abou Jamra, Rami
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110774/
https://www.ncbi.nlm.nih.gov/pubmed/33547425
http://dx.doi.org/10.1038/s41431-020-00803-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110774/
https://www.ncbi.nlm.nih.gov/pubmed/33547425
http://dx.doi.org/10.1038/s41431-020-00803-8

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