Whole Exome Sequencing Identifies CRB1 Defect in an Unusual Maculopathy Phenotype

Tsang SH, Burke T, Oll M, Yzer S, Lee W, Xie YA, Allikmets R. Whole Exome Sequencing Identifies CRB1 Defect in an Unusual Maculopathy Phenotype. Ophthalmology. 2014 May 6. [Epub ahead of print].