Your search returned 3 results.

Results
	1.	Polymorphic corneal amyloidosis: a disorder due to a novel mutation in the transforming growth factor beta-induced (BIGH3) gene. [electronic resource] by Eifrig, David E Afshari, Natalie A Buchanan, Harry W Bowling, Brandy L Klintworth, Gordon K Producer: 20040628 In: Ophthalmology vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Two cases of Reis-Bücklers corneal dystrophy (granular corneal dystrophy type III) caused by spontaneous mutations in the TGFBI gene. [electronic resource] by Tanhehco, Tasha Y Eifrig, David E Schwab, Ivan R Rapuano, Christopher J Klintworth, Gordon K Producer: 20060425 In: Archives of ophthalmology (Chicago, Ill. : 1960) vol. 124 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Atypical asymmetric lattice corneal dystrophy associated with a novel homozygous mutation (Val624Met) in the TGFBI gene. [electronic resource] by Afshari, Natalie A Bahadur, Rosanna P Eifrig, David E Thogersen, Ida B Enghild, Jan J Klintworth, Gordon K Producer: 20080520 In: Molecular vision vol. 14 Availability: No items available. Save to lists Add to cart (remove)

Refine your search