SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis
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概要
- 論文の詳細を見る
- 2009-05-01
著者
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Riazuddin Sheikh
Allama Iqbal Medical College-jinnah Hospital Complex University Of Health Sciences
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AHMED Zubair
Laboratory of Molecular Genetics, Division of Pediatric Otolaryngology Head and Neck Surgery, Cincinnati Children Hospital Research Foundation
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Riazuddin Saima
Laboratory Of Molecular Genetics Division Of Pediatric Otolaryngology Head And Neck Surgery Cincinnati Children Hospital Research Foundation
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Friedman Thomas
Section On Human Genetics Laboratory Of Molecular Genetics National Institute On Deafness And Other Communication Disorders National Institutes Of Health
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Ahmed Zubair
Laboratory Of Molecular Genetics Division Of Pediatric Otolaryngology Head And Neck Surgery Cincinnati Children Hospital Research Foundation
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Griffith Andrew
Otolaryngology Branch National Institute On Deafness And Other Communication Disorders National Institutes Of Health
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ANWAR Saima
National Center of Excellence in Molecular Biology, Punjab University
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TASNEEM Saba
National Center of Excellence in Molecular Biology, Punjab University
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JALEEL Ateeq-ul
National Center of Excellence in Molecular Biology, Punjab University
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KHAN Shahid
National Center of Excellence in Molecular Biology, Punjab University
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FRIEDMAN Thomas
Laboratory of Molecular Genetics, Section on Human Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health
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RIAZUDDIN Sheikh
National Center of Excellence in Molecular Biology, Punjab University
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Khan Shahid
National Center Of Excellence In Molecular Biology Punjab University
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Anwar Saima
National Center Of Excellence In Molecular Biology Punjab University
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Tasneem Saba
National Center Of Excellence In Molecular Biology Punjab University
関連論文
- Molecular and clinical studies of X-linked deafness among Pakistani families
- Amino acid 572 in TMC1 : hot spot or critical functional residue for dominant mutations causing hearing impairment
- Evidence for a founder mutation causing DFNA5 hearing loss in East Asians
- SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis
- Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population