Kent W Small et al.
Ophthalmology, 123(1), 9-18 (2015-10-29)
To identify specific mutations causing North Carolina macular dystrophy (NCMD). Whole-genome sequencing coupled with reverse transcription polymerase chain reaction (RT-PCR) analysis of gene expression in human retinal cells. A total of 141 members of 12 families with NCMD and 261