Cite
HARVARD Citation
Wolf, A. et al. (2017). A Novel Mutation in SLC26A4 Causes Nonsyndromic Autosomal Recessive Hearing Impairment. Otology & neurotology. 38 (2), pp. 173-179. [Online].
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Wolf, A. et al. (2017). A Novel Mutation in SLC26A4 Causes Nonsyndromic Autosomal Recessive Hearing Impairment. Otology & neurotology. 38 (2), pp. 173-179. [Online].