Identification and clinical implications of a novel pathogenic variant in the GJB2 gene causes autosomal recessive non-syndromic hearing loss in a consanguineous Iranian family
2020 ◽
Vol 9
(1)
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pp. 30-34
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2005 ◽
Vol 137A
(3)
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pp. 255-258
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2017 ◽
Vol 97
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pp. 113-126
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2020 ◽
1997 ◽
Vol 117
(3)
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pp. 337-342
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1996 ◽
Vol 116
(4)
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pp. 521-527
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2020 ◽