Generation of the first Autosomal Dominant Osteopetrosis Type II (ADO2) disease models

Autosomal Dominant Osteopetrosis Type II (ADO2) is a heritable osteosclerotic disorder dependent on osteoclast impairment. In most patients it results from heterozygous missense mutations in the chloride channel 7 (CLCN7) gene, encoding for a 2Cl(−)/1H(+) antiporter. By a knock-in strategy inserting...

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Bibliografiset tiedot
Päätekijät: Alam, Imranul, Gray, Amie K., Chu, Kang, Ichikawa, Shoji, Mohammad, Khalid S., Capannolo, Marta, Capulli, Mattia, Maurizi, Antonio, Muraca, Maurizio, Teti, Anna, Econs, Michael J., Fattore, Andrea Del
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2013
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3889206/
https://ncbi.nlm.nih.gov/pubmed/24185277
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2013.10.021
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