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JAMAOPHTHALMOL.2014.6115
JAMAOPHTHALMOL.2014.6115
http://dx.doi.org/10.1001/JAMAOPHTHALMOL.2014.6115
Founder Effect of a c.828+3A>T Splice Site Mutation in Peripherin 2 (PRPH2) Causing Autosomal Dominant Retinal Dystrophies.
P356
Q35667416-536F6573-3D46-4DD4-9E66-2F7DA59E84B0
P356
JAMAOPHTHALMOL.2014.6115
http://dx.doi.org/10.1001/JAMAOPHTHALMOL.2014.6115