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Identification of a novel dentin matrix protein-1 (DMP-1) mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia
Bone , 10/21/09
Turan S et al. – The identified genetic mutation underscores the importance of DMP–1 mutations in the pathogenesis of ARHP. Furthermore, DMP–1 mutations appear to contribute, through yet unknown mechanisms, to tooth development.
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