Document is current

Any future updates will be listed below

Enhanced but hypofunctional osteoclastogenesis in an autosomal dominant osteopetrosis type II case carrying a c.1856C>T mutation in CLCN7

Crossref DOI link: https://doi.org/10.1038/boneres.2016.35

Published Online: 2016-11-29

Update policy: https://doi.org/10.1007/springer_crossmark_policy

About CrossMark