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Myo1c mutations associated with hearing loss cause defects in the interaction with nucleotide and actin

โœ Scribed by Nancy Adamek; Michael A. Geeves; Lynne M. Coluccio


Book ID
105759298
Publisher
Springer
Year
2010
Tongue
English
Weight
616 KB
Volume
68
Category
Article
ISSN
1420-682X

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## Abstract Several mitochondrial DNA variants increase risk for developing sensorineural hearing loss following exposure to aminoglycoside antibiotics, a particular concern in the premature infant population, as many of these babies spend time in neonatal intensive care units and are treated with