Mutation analysis of the cathepsin C gene in Indian families with Papillon-Lefèvre syndrome

<p>Abstract</p> <p>Background</p> <p>PLS is a rare autosomal recessive disorder characterized by early onset periodontopathia and palmar plantar keratosis. PLS is caused by mutations in the cathepsin C (<it>CTSC</it>) gene. Dipeptidyl-peptidase I encoded by...

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Main Authors: Srivastava Satish (Author), Sethuraman Gomathy (Author), Sathyan Parthasarathy (Author), Prasad Pullabatla (Author), Markandaya Manjunath (Author), Selvaraju Veeriah (Author), Thakker Nalin (Author), Kumar Arun (Author)
Format: Book
Published: BMC, 2003-07-01T00:00:00Z.
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