Exome sequencing identified rare variants in genes HSPG2 and ATP2B4 in a family segregating developmental dysplasia of the hip

BACKGROUND: Developmental dysplasia of the hip (DDH) is a common pathological condition of the musculoskeletal system in infants which results in a congenital and developmental malformation of the hip joint. DDH is a spectrum of pathologies affecting the infant hip ranging from asymptomatic subtle r...

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Detalles Bibliográficos
Autores principales: Basit, Sulman, Albalawi, Alia M., Alharby, Essa, Khoshhal, Khalid I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5361705/
https://www.ncbi.nlm.nih.gov/pubmed/28327142
http://dx.doi.org/10.1186/s12881-017-0393-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5361705/
https://www.ncbi.nlm.nih.gov/pubmed/28327142
http://dx.doi.org/10.1186/s12881-017-0393-8

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