Cite
HARVARD Citation
Pangrazio, A. et al. (n.d.). SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity. Journal of bone and mineral research. pp. 1041-1049. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Pangrazio, A. et al. (n.d.). SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity. Journal of bone and mineral research. pp. 1041-1049. [Online].