HuGE Literature Finder
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Records 1-2
Evidence for the absence of mutations at GJB3, GJB4 and LOR in progressive symmetrical erythrokeratodermia.
Clinical and experimental dermatology 2011 Jun 36 (4): 399-405. Wei S, Zhou Y, Zhang T D, Huang Z M, Zhang X B, Zhu H L, Liang B H, Lin L, Deng |
Lack of association between Connexin 31 (GJB3) alterations and sensorineural deafness in Austria.
Hearing research 2004 Aug 194 (1-2): 81-6. Frei Klemens, Ramsebner Reinhard, Hamader Gertrude, Lucas Trevor, Schoefer Christian, Baumgartner Wolf-Dieter, Wachtler Franz J, Kirschhofer Kar |
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- Page last updated:Dec 5, 2019
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