Mutations in the connexin26/GJB2 gene are the most common event in non-syndromic hearing loss among the German population
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2011 ◽
Vol 75
(12)
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pp. 1572-1575
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2021 ◽
Vol 24
(1)
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pp. 50-61
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2018 ◽
Vol 147
(6)
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pp. 615
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2010 ◽
Vol 74
(9)
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pp. 1089-1091
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2013 ◽
Vol 33
(2)
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pp. 310-316
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2001 ◽
Vol 38
(10)
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pp. 36e-36
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2003 ◽
Vol 63
(6)
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pp. 516-521
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