P. Rausch

Further evidence for linkage of low–mid frequency hearing impairment to the candidate region on chromosome 4p16.3

A. Ziegler, J. Kunz, I. Böddeker, 2001, Clinical genetics.

Identification of a novel mutation in WFS1 in a family affected by low-frequency hearing impairment.

S. Uebe, J. Kunz, Benjamin Marquez-Klaka, 2003, Mutation research.

Evaluation of Cx26/GJB2 in German hearing impaired persons: mutation spectrum and detection of disequilibrium between M34T (c.101T>C) and ‐493del10

K. Lange, K. Sperling, B. Zoll, 2003, Human mutation.