OMIM/600965[Secondary Source ID] - Search Results

This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Add to My Bibliography

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Email: (change)

Frequency:

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

Results by year

Year	Number of Results
2003	1
2004	1
2025	0

2 results

Page of 1

Results by year

Page 1

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

Kunz J, Marquez-Klaka B, Uebe S, Volz-Peters A, Berger R, Rausch P. Kunz J, et al. Mutat Res. 2003 Apr 9;525(1-2):121-4. doi: 10.1016/s0027-5107(02)00265-8. Mutat Res. 2003. PMID: 12650912

Disruption of the WFS1 gene in mice causes progressive beta-cell loss and impaired stimulus-secretion coupling in insulin secretion.

Ishihara H, Takeda S, Tamura A, Takahashi R, Yamaguchi S, Takei D, Yamada T, Inoue H, Soga H, Katagiri H, Tanizawa Y, Oka Y. Ishihara H, et al. Hum Mol Genet. 2004 Jun 1;13(11):1159-70. doi: 10.1093/hmg/ddh125. Epub 2004 Mar 31. Hum Mol Genet. 2004. PMID: 15056606

Page of 1

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Results by year

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

2 results

Results by year

Search Page

Filters

My Custom Filters

Results by year

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

2 results

Results by year