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JCMM.13454
JCMM.13454
http://dx.doi.org/10.1111/JCMM.13454
Identification of a novel RPGRIP1 mutation in an Iranian family with leber congenital amaurosis by exome sequencing.
P356
Q47343102-ABA5022F-60B0-4446-B9E9-AD78BDACEBDB
P356
JCMM.13454
http://dx.doi.org/10.1111/JCMM.13454