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New compound heterozygous USH2A mutations in Usher syndrome.
Kuang, Longhao; Chen, Qingshan; Gan, Run; Yan, Xiaohe.
Affiliation
  • Kuang L; Shenzhen Key Laboratory of Ophthalmology, Shenzhen Eye Hospital, Jinan University, Shenzhen, China.
  • Chen Q; School of Optometry, Shenzhen University, Shenzhen, China.
  • Gan R; Shenzhen Key Laboratory of Ophthalmology, Shenzhen Eye Hospital, Jinan University, Shenzhen, China.
  • Yan X; School of Optometry, Shenzhen University, Shenzhen, China.
Acta Ophthalmol ; 98(1): e134-e135, 2020 Feb.
Article in En | MEDLINE | ID: mdl-30390381
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA / Extracellular Matrix Proteins / Usher Syndromes / Mutation Type of study: Diagnostic_studies Limits: Adult / Female / Humans Language: En Journal: Acta Ophthalmol Journal subject: OFTALMOLOGIA Year: 2020 Document type: Article Affiliation country: China
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA / Extracellular Matrix Proteins / Usher Syndromes / Mutation Type of study: Diagnostic_studies Limits: Adult / Female / Humans Language: En Journal: Acta Ophthalmol Journal subject: OFTALMOLOGIA Year: 2020 Document type: Article Affiliation country: China