CRB1 heterozygotes with regional retinal dysfunction: implications for genetic testing of leber congenital amaurosis.
Yzer S, Fishman GA, Racine J, Al-Zuhaibi S, Chakor H, Dorfman A, Szlyk J, Lachapelle P, van den Born LI, Allikmets R, Lopez I, Cremers FP, Koenekoop RK.
Yzer S, et al. Among authors: dorfman a.
Invest Ophthalmol Vis Sci. 2006 Sep;47(9):3736-44. doi: 10.1167/iovs.05-1637.
Invest Ophthalmol Vis Sci. 2006.
PMID: 16936081