Results 201 to 208 of about 5,313 (208)

Molecular detection of novel WFS1 mutations in patients with Wolfram syndrome by a DHPLC-based assay

Human Mutation, 2003
Alessandro de Luca, Bruno Dallapiccola, Silvana Briuglia   +2 more
exaly  

Relation between increased anxiety and reduced expression of alpha1 and alpha2 subunits of GABAA receptors in Wfs1-deficient mice

Neuroscience Letters, 2009
Eero Vasar, Sulev Koks, Hendrik Luuk
exaly  

Mutations in the WFS1 gene and low frequency hearing loss

Otolaryngology - Head and Neck Surgery, 2009
Matthew Whitley, Megha Garg, Xue Liu, Xiaomei Ouyang   +3 more
openaire   +1 more source

Wolfram syndrome and WFS1 gene

Clinical Genetics, 2011
exaly  

Mice heterozygous for WFS1 gene as mouse models for depression

2003
ROBERDS STEVEN L, HUFF RITA M
openaire   +3 more sources

Gene symbol: WFS1. Disease: Wolfram syndrome.

Human genetics, 2008
Polina, Tsygankova, E Yu, Zakharova, D P, Stepina   +2 more
openaire   +1 more source

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

Diabetic Medicine, 2008
exaly  

WFS1 geeni uurimine seoses skisofreeniaga

2013
openaire   +1 more source