Publication | Open Access

Novel Point Mutations, Deletions, and Polymorphisms in the Cathepsin C Gene in Nine Families from Europe and North Africa with Papillon–Lefèvre Syndrome

Genetic DisorderGeneticsPathogenesisGenetic EpidemiologyPathologyMolecular GeneticsNovel Point MutationsDisease Gene IdentificationGenomicsMedical GeneticsMedicineCathepsin C GeneNorth Africa