Genética Médica Querétaro,
Deep-intronic variants in ABCA4 suggest new therapeutic approaches for some patients with Stargardt disease https://goo.gl/yWYtRT…
Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides
Overview of attention for article published in Genetics in Medicine, January 2019
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In the top 5% of all research outputs scored by Altmetric
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High Attention Score compared to outputs of the same age (94th percentile)
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High Attention Score compared to outputs of the same age and source (86th percentile)
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