Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II
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概要
- 論文の詳細を見る
- 2009-12-01
著者
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Du Li
Department Of Medical Genetics Zhongshan School Of Medicine Sun Yat-sen University
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Yan Denise
Department Of Obstetrics And Gynecology Chinese Pla General Hospital
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Ouyang Xiaomei
Department Of Otolaryngology University Of Miami
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Du Li
Department Of Otolaryngology University Of Miami
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Liu Xue-zhong
Department Of Otolaryngology University Of Miami
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Jacobson Samuel
Department Of Ophthalmology Scheie Eye Institute University Of Pennsylvania
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Patterson D
Department Of Otolaryngology University Of Miami
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Patterson D.
Department of Otolaryngology, University of Miami
関連論文
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- Xp22.3 microdeletions in three Chinese families with X-linked ichthyosis
- Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China
- Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II
- Genetics and pathological mechanisms of Usher syndrome
- Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease
- The genetic bases for non-syndromic hearing loss among Chinese