Corinne Collet
0000-0001-6990-863X
64 papers found
Refreshing results…
Paget's disease of bone in the French population: novel SQSTM1 mutations, functional analysis, and genotype-phenotype correlations.
[Molecular analysis of Paget's disease of bone]
Stepwise control of osteogenic differentiation by 5-HT(2B) receptor signaling: nitric oxide production and phospholipase A2 activation.
Genetics of Paget's disease of bone.
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