USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1
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概要
- 論文の詳細を見る
- 2012-10-01
著者
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Khan Shaheen
National Center Of Excellence In Molecular Biology University Of The Punjab
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AHMED Zubair
Division of Pediatric Ophthalmology, Cincinnati Children's Hospital Medical Center
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RIAZUDDIN Saima
Division of Pediatric Ophthalmology, Cincinnati Children's Hospital Medical Center
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BHATTI Rashid
Division of Pediatric Ophthalmology, Cincinnati Children's Hospital Medical Center
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JAWOREK Thomas
Division of Pediatric Ophthalmology, Cincinnati Children's Hospital Medical Center
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LATIEF Noreen
National Center of Excellence in Molecular Biology, University of the Punjab
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JAWOREK Thomas
Division of Pediatric Ophthalmology, Cincinnati Children's Hospital Medical Center
関連論文
- Molecular and clinical studies of X-linked deafness among Pakistani families
- USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1
- Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population