CRELD1 variants are associated with bicuspid aortic valve in Turner syndrome

Turner syndrome (TS) is a chromosomal disorder caused by complete or partial loss of the second sex chromosome and exhibits phenotypic heterogeneity, even after accounting for mosaicism and karyotypic variation. Congenital heart defects (CHD) are found in up to 45 percent of girls with TS and span a...

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Detalles Bibliográficos
Autores principales: Pinnaro, Catherina T., Beck, Chloe B., Major, Heather J., Darbro, Benjamin W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10060348/
https://www.ncbi.nlm.nih.gov/pubmed/36929416
http://dx.doi.org/10.1007/s00439-023-02538-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10060348/
https://www.ncbi.nlm.nih.gov/pubmed/36929416
http://dx.doi.org/10.1007/s00439-023-02538-0

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