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PDFOriginal article
Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)
- Correspondence to: K W Kjaer Wilhelm Johannsen Centre for Functional Genome Research, Institute of Medical Biochemistry and Genetics, Panum Institute 24.4, 2200 Copenhagen N, Denmark; klausmedgen.ku.dk
Citation
Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)
Publication history
- Accepted November 18, 2004
- First published April 1, 2005.
Online issue publication
April 27, 2016
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Copyright 2005 Journal of Medical Genetics