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: | , , , , , , , |
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| Format: | Book |
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BMC,
2003-07-01T00:00:00Z.
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