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Prevalence of Cx26 (GJB2) gene mutation causing recessive nonsyndromic hearing impairment in India
Journal
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- Int. J. Hum. Genet.
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Int. J. Hum. Genet. 5 241-246, 2005
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Details 詳細情報について
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- CRID
- 1570291225818483712
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- NII Article ID
- 10030737656
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- Data Source
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- CiNii Articles