Mutations in osteoprotegerin account for the CCAL1 locus in calcium pyrophosphate deposition disease

OBJECTIVE: Mutations on chromosomes 5p (CCAL2) and 8q (CCAL1) have been linked to familial forms of calcium pyrophosphate deposition disease (CPDD). Mutations in the ANKH gene account for CCAL2, but the identity of CCAL1 has been elusive. Recently, a single Dutch kindred with a mutation in the Tumor...

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Pubblicato in:Osteoarthritis Cartilage
Autori principali: Williams, C.J., Qazi, U., Bernstein, M., Charniak, A., Gohr, C., Mitton-Fitzgerald, E., Ortiz, A., Cardinal, L., Kaell, A.T., Rosenthal, A.K.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2018
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6293976/
https://ncbi.nlm.nih.gov/pubmed/29578045
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.joca.2018.03.005
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