4.3 Article

Autosomal dominant transmission of diabetes and congenital hearing impairment secondary to a missense mutation in the WFS1 gene

Related references

Note: Only part of the references are listed.
Article Biotechnology & Applied Microbiology

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

J Kunz et al.

MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS (2003)

Article Medicine, General & Internal

Maternally inherited diabetes and deafness: A multicenter study

PJ Guillausseau et al.

ANNALS OF INTERNAL MEDICINE (2001)