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De Novo Mutation in X-Linked Hearing Loss-Associated POU3F4 in a Sporadic Case of Congenital Hearing Loss. http://t.co/Emn4kSWuTe
De Novo Mutation in X-Linked Hearing Loss–Associated POU3F4 in a Sporadic Case of Congenital Hearing Loss
Overview of attention for article published in Annals of Otology, Rhinology & Laryngology, March 2015
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About this Attention Score
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Above-average Attention Score compared to outputs of the same age (63rd percentile)
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Good Attention Score compared to outputs of the same age and source (76th percentile)
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