A novel connexin 26 gene mutation associated with features of the keratitis-ichthyosis-deafness syndrome and the follicular occlusion triad
Author:
Publisher
Elsevier BV
Subject
Dermatology
Reference22 articles.
1. Connexin mutations in skin disease and hearing loss;Kelsell;Am J Hum Genet,2001
2. Connexins: a connection with the skin;Richard;Exp Dermatol,2000
3. Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins;Rabionet;Hum Mutat,2000
4. A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families;Maestrini;Hum Mol Genet,1999
5. A novel connexin 26 mutation in a patient diagnosed with keratitis-ichthyosis-deafness syndrome;van Steensel;J Invest Dermatol,2002
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