On the association between Chiari malformation type 1, bone mineral density and bone related genes
BACKGROUND: Chiari malformation type 1 (C1M) is a neurological disease characterized by herniation of the cerebellar tonsils below the foramen magnum. Cranial bone constriction is suspected to be its main cause. To date, genes related to bone development (e.g. DKK1 or COL1A2) have been associated wi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933671/ https://www.ncbi.nlm.nih.gov/pubmed/35313637 http://dx.doi.org/10.1016/j.bonr.2022.101181 |