SIR, Papillon\u2013Lefe`vre syndrome (PLS) is an autosomal recessivegenodermatosis mainly characterized by early-onset periodontitisand palmoplantar keratoderma. Recurrent pyogenic skininfections, usually of mild degree and self-healing, are relativelycommon additional features.1,2 PLS is caused by lossof-function mutations in the CTSC gene, which encodes forcathepsin C, a lysosomal cysteine protease required forthe activation of granule-associated serine proteases inimmune \u2044inflammatory cells
AbstractPapillon–Lefevre syndrome (PLS) is a very rare, autosomal recessive syndrome characterized b...
The Papillon–Lefèvre syndrome, inherited in an autosomal recessive pattern, manifests with palmoplan...
Papillon-Lefevre syndrome (PLS) is an autosomal recessive disorder characterised by severe early ons...
SIR, Papillon\u2013Lefe`vre syndrome (PLS) is an autosomal recessivegenodermatosis mainly characteri...
Papillon-Lefevre syndrome (PLS) is an autosomal recessive disorder characterised by palmoplantar hyp...
Papillon-Lefevre syndrome is an autosomal recessive genodermatosis typically manifesting with the co...
Papillon-Lefevre syndrome (PLS) is an inherited human disease characterized by early-onset periodont...
AbstractBackgroundCathepsin C gene (CTSC) (MIM#602365) is a lysosomal cysteine proteinase coding gen...
Introduction-Papillon-Lefevre syndrome (PLS) is an autosomal recessive disorder characterised by pal...
Background Cathepsin C gene (CTSC) (MIM#602365) is a lysosomal cysteine proteinase coding gene which...
Papillon Lefevre syndrome is an extremely rare autosomal recessive disorder characterized by diffuse...
Papillon-Lefëvre syndrome (PLS), classified as ectodermal dysplasia, is an autosomal recessive condi...
Papillon-Lefevre syndrome (PLS) is an autosomal recessive palmoplantar keratoderma caused by catheps...
Papillon-Lefevre Syndrome (PLS) is (OMIM 245'000) a rare genodermatosis, transmitted in an autosomal...
Papillon–Lefèvre syndrome is an autosomal recessive disorder characterized by palmoplantar keratoder...
AbstractPapillon–Lefevre syndrome (PLS) is a very rare, autosomal recessive syndrome characterized b...
The Papillon–Lefèvre syndrome, inherited in an autosomal recessive pattern, manifests with palmoplan...
Papillon-Lefevre syndrome (PLS) is an autosomal recessive disorder characterised by severe early ons...
SIR, Papillon\u2013Lefe`vre syndrome (PLS) is an autosomal recessivegenodermatosis mainly characteri...
Papillon-Lefevre syndrome (PLS) is an autosomal recessive disorder characterised by palmoplantar hyp...
Papillon-Lefevre syndrome is an autosomal recessive genodermatosis typically manifesting with the co...
Papillon-Lefevre syndrome (PLS) is an inherited human disease characterized by early-onset periodont...
AbstractBackgroundCathepsin C gene (CTSC) (MIM#602365) is a lysosomal cysteine proteinase coding gen...
Introduction-Papillon-Lefevre syndrome (PLS) is an autosomal recessive disorder characterised by pal...
Background Cathepsin C gene (CTSC) (MIM#602365) is a lysosomal cysteine proteinase coding gene which...
Papillon Lefevre syndrome is an extremely rare autosomal recessive disorder characterized by diffuse...
Papillon-Lefëvre syndrome (PLS), classified as ectodermal dysplasia, is an autosomal recessive condi...
Papillon-Lefevre syndrome (PLS) is an autosomal recessive palmoplantar keratoderma caused by catheps...
Papillon-Lefevre Syndrome (PLS) is (OMIM 245'000) a rare genodermatosis, transmitted in an autosomal...
Papillon–Lefèvre syndrome is an autosomal recessive disorder characterized by palmoplantar keratoder...
AbstractPapillon–Lefevre syndrome (PLS) is a very rare, autosomal recessive syndrome characterized b...
The Papillon–Lefèvre syndrome, inherited in an autosomal recessive pattern, manifests with palmoplan...
Papillon-Lefevre syndrome (PLS) is an autosomal recessive disorder characterised by severe early ons...
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