T. Cater

Pharmacological rescue of noise induced hearing loss using N-acetylcysteine and acetyl-l-carnitine

R. Kopke, Ronald L. Jackson, Jianzhong Liu, 2007, Hearing Research.

Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15

T. Walsh, M. King, B. Fernandez, 2009, European Journal of Human Genetics.

Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1.

M. King, B. Fernandez, Ming K. Lee, 2001, Human molecular genetics.