Genetic variants in TRPM7 associated with unexplained stillbirth modify ion channel function

Stillbirth is the loss of a fetus after 22 weeks of gestation, of which almost half go completely unexplained despite post-mortem. We recently sequenced 35 arrhythmia-associated genes from 70 unexplained stillbirth cases. Our hypothesis was that deleterious mutations in channelopathy genes may have...

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Detalles Bibliográficos
Autores principales: Cartwright, James H, Aziz, Qadeer, Harmer, Stephen C, Thayyil, Sudhin, Tinker, Andrew, Munroe, Patricia B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
General Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7372550/
https://www.ncbi.nlm.nih.gov/pubmed/31423533
http://dx.doi.org/10.1093/hmg/ddz198

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7372550/
https://www.ncbi.nlm.nih.gov/pubmed/31423533
http://dx.doi.org/10.1093/hmg/ddz198

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