Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutation

Prepubertal periodontitis (PPP) is a rare and rapidly progressive disease of young children that results in destruction of the periodontal support of the primary dentition. The condition may occur as part of a recognised syndrome or may occur as an isolated finding. Both autosomal dominant and reces...

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Veröffentlicht in:Journal of medical genetics 2000-02, Vol.37 (2), p.95-101
Hauptverfasser: Hart, T C, Hart, P S, Michalec, M D, Zhang, Y, Marazita, M L, Cooper, M, Yassin, O M, Nusier, M, Walker, S
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Sprache:eng
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