Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome).
Kjaer, K. W.; Hansen, L.; Schwabe, G. C.; Marques-de-Faria, A. P.; Eiberg, H.; Mundlos, S.; Tommerup, N.; Rosenberg, T.; Journal of Medical Genetics, 2005, vol. 42, issue 4, p 292, ISSN 00222593. ISBN 14686244.

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