Skip to main content

USH1C Products

USH1C may be involved in protein-protein interaction. Defects in USH1C are the cause of Usher syndrome type 1c. It is an autosomal recessive sensory defect involving congenital profound sensorineural deafness, vestibular dysfunction, and blindness due to progressive retinitis pigmentosa. Defects in USH1C are also the cause of nonsyndromic recessive...
Show More

1 result for "USH1C" in Products

1 result for "USH1C" in Products

USH1C Products

USH1C may be involved in protein-protein interaction. Defects in USH1C are the cause of Usher syndrome type 1c. It is an autosomal recessive sensory defect involving congenital profound sensorineural deafness, vestibular dysfunction, and blindness due to progressive retinitis pigmentosa. Defects in USH1C are also the cause of nonsyndromic recessive...
Show More
Catalog #: NBP3-38088PE
Applications: WB, ELISA
Reactivity: Human, Mouse, Rat
Results Per Page
5 10 25 50
/ 1
Select 2 to 4 Items to Compare
 
 
 
 
×