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Literature for OMIM 600791: DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT; DFNB4
Xenbase Articles:
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Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations., Bockenhauer D,Stanescu HC,Bandulik S,Zdebik AA,Reichold M,Tobin J,Lieberer E,Landoure G,Arora R,Sirimanna T,Thompson D,Cross JH,Al Masri O,Tullus K,Yeung S,Anikster Y,Hubank M,Dillon MJ,Arcos-Burgos M,Knepper MA,Dobbie A,Gahl WA,Warth R,Sheridan E,Kleta R,Sterner C,Klootwijk E,van't Hoff W,Feather S,Heitzmann D, N Engl J Med. May 7, 2009; 360(19):1533-4406. |
Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndrome.,
Yang T,Gurrola JG,Wu H,Chiu SM,Wangemann P,Snyder PM,Smith RJ,
Am J Hum Genet. May 1, 2009; 84(5):1537-6605.
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Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes.,
Neal SJ,Rajasekaran A,Jusić N,Taylor L,Read M,Alfandari D,Alfandari D,Pignoni F,Moody SA,
J Exp Zool B Mol Dev Evol. May 1, 2024; 342(3):1552-5015.
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