De novo mutation in the gene encoding connexin‐26 (GJB2) in a sporadic case of keratitis‐ichthyosis‐deafness (KID) syndrome
- 24 September 2002
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics Part A
- Vol. 117A (1), 89-91
- https://doi.org/10.1002/ajmg.a.10851
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
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