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

Open

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