Phenotype–genotype correlations in a pseudodominant Stargardt disease pedigree due to a novel ABCA4 deletion–insertion variant causing a splicing defect
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I. Constable | F. Chen | S. Wilton | S. Fletcher | Jason Charng | A. Adams | M. Aung-Htut | Jennifer A. Thompson | T. Lamey | T. McLaren | J. D. De Roach | S. McLenachan | E. Chelva | Dan Zhang | S. Chen | Di Huang | J. Charng