Evidence of a founder effect for four cathepsin C gene mutations in Papillon-Lefèvre syndrome patients
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A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1Mutation analysis of the cathepsin C gene in Indian families with Papillon-Lefèvre syndromeCTSC and Papillon-Lefèvre syndrome: detection of recurrent mutations in Hungarian patients, a review of published variants and database updatePapillon-Lefevre syndrome: Reporting consanguinity as a risk factorThe Surgeon General's Report and special-needs patients: a framework for action for children and their caregivers.Risk factors for periodontitis in children and young persons.Inheritance of occlusal topography: a twin study.Heritability of oral microbial species in caries-active and caries-free twins.Proxy molecular diagnosis from whole-exome sequencing reveals Papillon-Lefevre syndrome caused by a missense mutation in CTSCGenes and gene polymorphisms associated with periodontal disease.Longitudinal analysis of heritability for dental caries traitsNovel cathepsin C mutation in a Brazilian family with Papillon-Lefèvre syndrome: case report and mutation updateThe genetic basis of periodontitis.Papillon-Lefèvre syndrome: a series of five cases among siblingsInherited diseases caused by mutations in cathepsin protease genes.Treatment responses to tooth whitening in twins.Whole-exome sequencing reveals a recurrent mutation in the cathepsin C gene that causes Papillon-Lefevre syndrome in a Saudi family.Evidence for a founder mutation in the cathepsin C gene in three families with Papillon-Lefèvre syndromeElevated hydroperoxide levels and antioxidant patterns in Papillon-Lefèvre syndrome.A novel mutation of the cathepsin C gene in Papillon-Lefèvre syndrome.Dental caries and microbial acid production in twins.A homozygous cathepsin C mutation associated with Haim-Munk syndrome.Orthodontic treatment in a patient with Papillon-Lefèvre syndrome.The role of cathepsin C in Papillon-Lefèvre syndrome, prepubertal periodontitis, and aggressive periodontitis.Cathepsin C Gene 5'-Untranslated Region Mutation in Papillon-Lefèvre Syndrome
P2860
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P2860
Evidence of a founder effect for four cathepsin C gene mutations in Papillon-Lefèvre syndrome patients
description
2001 nî lūn-bûn
@nan
2001 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Evidence of a founder effect f ...... llon-Lefèvre syndrome patients
@ast
Evidence of a founder effect f ...... llon-Lefèvre syndrome patients
@en
Evidence of a founder effect f ...... llon-Lefèvre syndrome patients
@nl
type
label
Evidence of a founder effect f ...... llon-Lefèvre syndrome patients
@ast
Evidence of a founder effect f ...... llon-Lefèvre syndrome patients
@en
Evidence of a founder effect f ...... llon-Lefèvre syndrome patients
@nl
prefLabel
Evidence of a founder effect f ...... llon-Lefèvre syndrome patients
@ast
Evidence of a founder effect f ...... llon-Lefèvre syndrome patients
@en
Evidence of a founder effect f ...... llon-Lefèvre syndrome patients
@nl
P2093
P2860
P356
P1476
Evidence of a founder effect f ...... llon-Lefèvre syndrome patients
@en
P2093
D N Tatakis
T Lundgren
P2860
P304
P356
10.1136/JMG.38.2.96
P407
P577
2001-02-01T00:00:00Z