Variants in the 5′UTR reduce SHOX expression and contribute to SHOX haploinsufficiency

SHOX haploinsufficiency causes 70–90% of Léri-Weill dyschondrosteosis (LWD) and 2–10% of idiopathic short stature (ISS). Deletions removing the entire gene or enhancers and point mutations in the coding region represent a well-established cause of haploinsufficiency. During diagnostic genetic testin...

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Detalles Bibliográficos
Autores principales: Babu, Deepak, Vannelli, Silvia, Fanelli, Antonella, Mellone, Simona, Baffico, Ave Maria, Corrado, Lucia, Essa, Wael Al, Grandone, Anna, Bellone, Simonetta, Monzani, Alice, Vinci, Giulia, De Sanctis, Luisa, Stuppia, Liborio, Prodam, Flavia, Giordano, Mara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852508/
https://www.ncbi.nlm.nih.gov/pubmed/32647378
http://dx.doi.org/10.1038/s41431-020-0676-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852508/
https://www.ncbi.nlm.nih.gov/pubmed/32647378
http://dx.doi.org/10.1038/s41431-020-0676-y

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