B. Charles Thomas

Learn More
PURPOSE To elucidate the basis of the autosomal dominant congenital nuclear cataracts caused by the connexin50 mutant, CX50R23T, by determining its cellular distribution and functional behavior and the consequences of substituting other amino acids for arginine-23. METHODS Connexin50 (CX50) mutants were generated by PCR and transfected into HeLa or N2a(More)
  • 1