A novel mutation in the connexin 26 gene ( GJB2) in a child with clinical and histological features of keratitis-ichthyosis-deafness (KID) syndrome.
| Autor: | Koppelhus, U.1 uffkop@rm.dk, Tranebjærg, L.2,3, Esberg, G.4, Ramsing, M.5, Lodahl, M.3, Rendtorff, N. D.3, Olesen, H. V.4, Sommerlund, M.1 |
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| Zdroj: | Clinical & Experimental Dermatology. Mar2011, Vol. 36 Issue 2, p142-148. 7p. 2 Color Photographs, 2 Diagrams, 1 Chart. |
| Databáze: | Academic Search Ultimate |
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