In vitro osteoclastogenesis from Gaucher patients' cells correlates with bone mineral density but not with Chitotriosidase
Gaucher disease (GD) is caused by mutations on the gene encoding for the lysosomal enzyme glucocerebrosidase. Type I GD (GD1) patients present anemia, hepatosplenomegaly and bone alterations. In spite of treatment, bone alterations in GD patients persist, including poor bone mineral density (BMD). M...
Guardado en:
| Autores principales: | Bondar, Constanza María, Mucci, Juan Marcos, Crivaro, Andrea Natalia, Ormazabal, Maximiliano Emanuel, Ceci, Romina, Oliveri, María Beatriz, González, D., Rozenfeld, Paula Adriana |
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| Formato: | Articulo Preprint |
| Lenguaje: | Inglés |
| Publicado: |
2017
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| Materias: | |
| Acceso en línea: | http://sedici.unlp.edu.ar/handle/10915/99804 https://ri.conicet.gov.ar/11336/47678 |
| Aporte de: |
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