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Prevalence of GBJ2 mutations in patients with severe to profound congenital nonsyndromic sensorineural hearing loss in Bulgarian population

✍ Scribed by Diana P. Popova; Radka Kaneva; Sonya Varbanova; Todor M. Popov

Book ID
113039978
Publisher
Springer-Verlag
Year
2011
Tongue
English
Weight
156 KB
Volume
269
Category
Article
ISSN
0302-9530

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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