Compound heterozygous MYO7A mutations segregating Usher syndrome type 2 in a Han family. [electronic resource]

By: Contributor(s): Producer: 20170313Description: 150-155 p. digitalISSN:
  • 1872-8464
Subject(s): Online resources: In: International journal of pediatric otorhinolaryngology vol. 90
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Publication Type: Journal Article

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