Homozygous and compound heterozygous MMP20 mutations in amelogenesis imperfecta.
about
Kallikrein-related peptidase-4 (KLK4): role in enamel formation and revelations from ablated miceDental enamel development: proteinases and their enamel matrix substratesAnalyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis ImperfectaEvolutionary Analysis Predicts Sensitive Positions of MMP20 and Validates Newly- and Previously-Identified MMP20 Mutations Causing Amelogenesis ImperfectaThe molecular basis of hereditary enamel defects in humans.A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvementMMP20 modulates cadherin expression in ameloblasts as enamel develops.Matrix metalloproteinase-20 over-expression is detrimental to enamel development: a Mus musculus modelAmelogenesis Imperfecta; Genes, Proteins, and Pathways.Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.Novel MMP20 and KLK4 Mutations in Amelogenesis Imperfecta.Ablation of Runx2 in Ameloblasts Suppresses Enamel Maturation in Tooth Development.
P2860
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P2860
Homozygous and compound heterozygous MMP20 mutations in amelogenesis imperfecta.
description
2013 nî lūn-bûn
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name
Homozygous and compound heterozygous MMP20 mutations in amelogenesis imperfecta.
@en
Homozygous and compound heterozygous MMP20 mutations in amelogenesis imperfecta.
@nl
type
label
Homozygous and compound heterozygous MMP20 mutations in amelogenesis imperfecta.
@en
Homozygous and compound heterozygous MMP20 mutations in amelogenesis imperfecta.
@nl
prefLabel
Homozygous and compound heterozygous MMP20 mutations in amelogenesis imperfecta.
@en
Homozygous and compound heterozygous MMP20 mutations in amelogenesis imperfecta.
@nl
P2093
P2860
P356
P1476
Homozygous and compound heterozygous MMP20 mutations in amelogenesis imperfecta
@en
P2093
C Schneider
E Karayigit
J Hemmerlé
P2860
P304
P356
10.1177/0022034513488393
P407
P577
2013-04-26T00:00:00Z