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Corrigendum
for Caronia et al.,
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CORRIGENDUM |
Caronia, G., Goodman, F. R., McKeown, C. M. E., Scambler, P. J. and Zappavigna, V. Development 130, 1701-1712.
While this article was in press, a phenotype similar to that described,
caused by an identical mutation, was identified by Johnson et al. in two
further families from the south-east of England
(Johnson et al., 2003
).
Microsatellite genotyping showed that the affected individuals from all three
families share the same haplotype across the HOXD cluster region, suggesting
that the mutation arose in a common ancestor (F.R.G., unpublished).
The authors apologise to readers for this omission.
REFERENCES
Johnson, D., Kan, S., Oldridge, M., Trembath, R. C., Roche, P.,
Esnouf, R. M., Giele, H. and Wilkie, A. O. M. (2003).
Missense mutations in the homeodomain of HOXD13 are associated with
brachydactyly types D and E. Am. J. Hum. Genet. (in
press).
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