Genetic Heterogeneity of KID Syndrome: Identification of a Cx30 Gene (GJB6) Mutation in a Patient with KID Syndrome and Congenital Atrichia
- 1 May 2004
- journal article
- case report
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 122 (5), 1108-1113
- https://doi.org/10.1111/j.0022-202x.2004.22518.x
Abstract
No abstract availableKeywords
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