Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees

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Brittany T. Truong, Talitha K.L. Yarza, Tori Bootpetch Roberts, Susannah Roberts, Jonathan Xu, Matthew J. Steritz, Celina A.M. Tobias-Grasso, Mahshid Azamian, Seema R. Lalani, Karen L. Mohlke, Nanette R. Lee, Eva Maria Cutiongco-de la Paz, Maria Rina T. Reyes-Quintos, Regie Lyn P. Santos-Cortez, Charlotte M. Chiong

2019 Clinical Genetics Vol. 95 Issue 5 Letter Cited by 12 Quartile

Abstract

[No abstract available]

Affiliations

Human Medical Genetics and Genomics Program, University of Colorado School of Medicine, Aurora, United States; Philippine National Ear Institute, University of the Philippines (UP) Manila-National Institutes of Health (NIH), Manila, Philippines; Newborn Hearing Screening Reference Center, UP Manila-NIH, Manila, Philippines; Department of Otolaryngology, University of Colorado School of Medicine, Aurora, United States; MED-EL, Innsbruck, Austria; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, United States; Department of Genetics, University of North Carolina, Chapel Hill, United States; Office of Population Studies Foundation and Department of Anthropology, Sociology and History, University of San Carlos, Cebu, Philippines; UP Manila-NIH, Manila, 1000, Philippines; Philippine Genome Center, Quezon City, Philippines; Department of Otorhinolaryngology, UP Manila College of Medicine-Philippine General Hospital, Manila, Philippines

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