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SREP14867
SREP14867
http://dx.doi.org/10.1038/SREP14867
SPP2 Mutations Cause Autosomal Dominant Retinitis Pigmentosa
P356
Q36149803-54C4022A-85DB-47FC-AE18-E745EFD79961
P356
SREP14867
http://dx.doi.org/10.1038/SREP14867