| 1 | GJB2, GJB6, KID, KID2
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| From Hyperactive Connexin26 Hemichannels to Impairments in Epidermal Calcium Gradient and Permeability Barrier in the Keratitis-Ichthyosis-Deafness Syndrome
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| García IE, Bosen F, Mujica P, Pupo A, Flores-Muñoz C, Jara O, González C, Willecke K, Martínez AD.
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| J Invest Dermatol. Mar;136(3):574-583. doi: 10.1016/j.jid.2015.11.017. Epub 2016 Jan 8. 2016
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| 2 | GJB6, KID2
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| Mutations in GJB6 causing phenotype resembling pachyonychia congenita.
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| Hale GI, Wilson NJ, Smith FJ, Wylie G, Schwartz ME, Zamiri M.
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| Br J Dermatol. 172(5):1447-9. doi: 10.1111/bjd.13520. Epub 2015 Mar 13 2015
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| 3 | GJB6, KID2
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| Genetic heterogeneity of KID syndrome: identification of a Cx30 gene (GJB6) mutation in a patient with KID syndrome and congenital atrichia.
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| Jan AY, Amin S, Ratajczak P, Richard G, Sybert VP.
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| J Invest Dermatol 122(5):1108-13. 2004
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