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Mitochondrial deafness

โœ Scribed by H Kokotas; MB Petersen; PJ Willems


Book ID
110888396
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
192 KB
Volume
71
Category
Article
ISSN
0009-9163

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Mitochondrial deafness mutations reviewe
โœ Nathan Fischel-Ghodsian ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 288 KB

The first molecular defect for nonsyndromic hearing loss was identified in 1993, and was a mitochondrial mutation. Since then a number of inherited mitochondrial DNA (mtDNA) mutations have been implicated in hearing loss, and acquired mtDNA mutations have been proposed as one of the causes of the he