Novel homozygous loss-of-function mutations in RP1 and RP1L1 genes in retinitis pigmentosa patients.
2019
ABSTRACTBackground: Retinitis pigmentosa (RP) is a heterogeneous group of ocular dystrophy. It is challenging to identify the underlying genetic defect in individuals with RP due to huge genetic he...
Keywords:
-
Correction
-
Source
-
Cite
-
Save
54
References
9
Citations
NaN
KQI