Founder Effect of a c.828+3A>T Splice Site Mutation in Peripherin 2 (PRPH2) Causing Autosomal Dominant Retinal Dystrophies.
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E. Stone | S. Daiger | S. Bowne | L. Sullivan | D. Birch | R. S. Ruiz | S. Shankar | D. Hughbanks-Wheaton | S. J. Bowne