Abstract: The gene responsible for an autosomal dominant con-rod retinal dystrophy is identified, TULP2. The genes are used to produce the encoded protein; in screening for compositions that modulate the expression or function of TULP2 protein; and in studying associated physiological pathways.
Type:
Grant
Filed:
September 4, 1996
Date of Patent:
January 6, 1998
Assignees:
Sequana Theraputics, Inc., Jackson Lab.
Inventors:
Michael North, Patsy Nishina, Juergen Naggert