A canonical splice site mutation in GIPC3 causes sensorineural hearing loss in a large Pakistani family.

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第一作者： Saima,Siddiqi

第一单位： Institute of Biomedical and Genetic Engineering (IBGE), Islamabad, Pakistan.

作者： Saima,Siddiqi ^[1] ; Muhammad,Ismail ^[1] ; Jaap,Oostrik ^[2] ; Saba,Munawar ^[3] ; Atika,Mansoor ^[1] ; Hannie,Kremer ^[4] ; Raheel,Qamar ^[5] ; Margit,Schraders ^[2]

作者单位： Institute of Biomedical and Genetic Engineering (IBGE), Islamabad, Pakistan. ^[1] 1] Department of Otorhinolaryngology, Head and Neck Surgery, Radboud University Medical Center, Nijmegen, The Netherlands [2] Radboud Institute for Molecular Life Sciences, Nijmegen, The Netherlands. ^[2] 1] Institute of Biomedical and Genetic Engineering (IBGE), Islamabad, Pakistan [2] Research Center For Modeling and Simulation, National University of Sciences and Technology (NUST), Islamabad, Pakistan. ^[3] 1] Department of Otorhinolaryngology, Head and Neck Surgery, Radboud University Medical Center, Nijmegen, The Netherlands [2] Radboud Institute for Molecular Life Sciences, Nijmegen, The Netherlands [3] Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands. ^[4] 1] COMSATS Institute of Information Technology, Islamabad, Pakistan [2] Al-Nafees Medical College and Hospital, Isra University, Islamabad, Pakistan. ^[5]