Evidence of a founder effect for four cathepsin C gene mutations in Papillon-Lefèvre syndrome patients

Por Zhang, Y, Lundgren, T, Renvert, S, Tatakis, D, Firatli, E, Uygur, C, Hart, P, Gorry, M, Marks, J, Hart, T
Publicado em 2001

Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects

Por Hart, T, Hart, P, Gorry, M, Michalec, M, Ryu, O, Uygur, C, Ozdemir, D, Firatli, S, Aren, G, Firatli, E
Publicado em 2003

Identification of cathepsin C mutations in ethnically diverse Papillon-Lefèvre syndrome patients

Por Hart, P, Zhang, Y, Firatli, E, Uygur, C, Lotfazar, M, Michalec, M, Marks, J, Lu, X, Coates, B, Seow, W, Marshall, R, Williams, D, Reed, J, Wright, J, Hart, T
Publicado em 2000