Liu et al., 2017
- Putative digenic inheritance of heterozygous RP1L1 and C2orf71 null mutations in syndromic retinal dystrophy.
Ophthalmic genetics
38(2):127-132
Full text @ Ophthalmic Genet.
| Marker Type | Symbol | Name |
|---|---|---|
| Gene | pcare1 | photoreceptor cilium actin regulator 1 |
| Gene | rp1l1a | rp1 like 1a |