S Xiao et al.
Nature Genet. 27, 201–204 (2001).
Due to printer error, one of the pedigrees in Fig. 1 and the legend were omitted. The complete figure is printed below.
Fig. 1 Pedigrees and haplotype analysis. In family B, the disease gene was mapped centromeric to the polymorphic marker SPP1. The disease gene in family C was localized to the interval defined by genes D4S1534 and D4S2623.
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The online version of the original article can be found at 10.1038/84848
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Erratum: Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP. Nat Genet 27, 345 (2001). https://doi.org/10.1038/85933
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DOI: https://doi.org/10.1038/85933
