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Frequency of mitochondrial DNA point mutations among patients with familial sensorineural hearing impairment

✍ Scribed by Lehtonen, Mervi S; Uimonen, Seija; Hassinen, Ilmo E; Majamaa, Kari


Book ID
110024950
Publisher
Nature Publishing Group
Year
2000
Tongue
English
Weight
65 KB
Volume
8
Category
Article
ISSN
1018-4813

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## Abstract ## Objectives/Hypothesis: To develop a cost‐effective and robust genetic diagnostic tool for patients with idiopathic nonsyndromic sensorineural hearing impairment. ## Study Design: Development of a diagnostic tool and validation in a prospective cohort. ## Methods: Twenty common s