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Copy number loss in the region of the ASPN gene in patients with acetabular dysplasia: ASPN CNV in acetabular dysplasia

OBJECTIVES: We have previously investigated an association between the genome copy number variation (CNV) and acetabular dysplasia (AD). Hip osteoarthritis is associated with a genetic polymorphism in the aspartic acid repeat in the N-terminal region of the asporin (ASPN) gene; therefore, the presen...

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Detalles Bibliográficos
Autores principales: Sekimoto, T., Ishii, M., Emi, M., Kurogi, S., Funamoto, T., Yonezawa, Y., Tajima, T., Sakamoto, T., Hamada, H., Chosa, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539304/
https://www.ncbi.nlm.nih.gov/pubmed/28747338
http://dx.doi.org/10.1302/2046-3758.67.BJR-2016-0094.R1