Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population
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概要
- 論文の詳細を見る
- 2013-02-01
著者
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Khan Shaheen
National Center Of Excellence In Molecular Biology University Of The Punjab
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Riazuddin Sheikh
Allama Iqbal Medical College-jinnah Hospital Complex University Of Health Sciences
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LATIEF Noreen
National Center of Excellence in Molecular Biology, University of the Punjab
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IQBAL Farheena
Center for Applied Molecular Biology
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RIAZUDDIN Saima
National Center of Excellence in Molecular Biology, University of the Punjab
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FRIEDMAN Thomas
Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders
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BASHIR Zil-e-Huma
National Center of Excellence in Molecular Biology, University of the Punjab
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BELYANTSEVA Inna
Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders
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RIAZUDDIN S
National Center of Excellence in Molecular Biology, University of the Punjab
関連論文
- Molecular and clinical studies of X-linked deafness among Pakistani families
- SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis
- 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