PuSH - Publication Server of Helmholtz Zentrum München

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1.
Seco, C.Z.* et al.: Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cells. Eur. J. Hum. Genet. 24, 542-549 (2016)
2.
Shafique, S.* et al.: Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families. PLoS ONE 9:e100146 (2014)