Genotyping with a 198 Mutation Arrayed Primer Extension Array for Hereditary Hearing Loss: Assessment of Its Diagnostic Value for Medical Practice

Open Access

Peer-reviewed

Research Article

Juan Rodriguez-Paris,

Affiliation Department of Pathology, Stanford University School of Medicine, Stanford, California, United States of America
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Lynn Pique,

Affiliation Department of Pathology, Stanford University School of Medicine, Stanford, California, United States of America
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Tahl Colen,

Affiliation California Ear Institute, Palo Alto, California, United States of America
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Joseph Roberson,

Affiliation California Ear Institute, Palo Alto, California, United States of America
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Phyllis Gardner,

Affiliation Department of Medicine, Stanford University School of Medicine, Stanford, California, United States of America
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Iris Schrijver

* E-mail: ischrijver@stanfordmed.org

Affiliations Department of Pathology, Stanford University School of Medicine, Stanford, California, United States of America, Department of Pediatrics, Stanford University School of Medicine, Stanford, California, United States of America
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Deafness
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Mutation detection
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Mutation
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Microarrays
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Heterozygosity
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Deletion mutation
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Insertion mutation
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Mitochondria
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