Genes
LRAT
OMIMLocus: 4q32.1
Protein: Lecithin retinol acyltransferase
Disorder(s):
- Retinal Dystrophy, Early-Onset, Severe
- LRAT-Related Leber Congenital Amaurosis
- LRAT-Related Retinitis Pigmentosa
Locus: 4q32.1
Protein: Lecithin retinol acyltransferase
Disorder(s):