Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction - Concepedia

Concepedia

Publication | Open Access

Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction

DOI Full Paper Access

27

Citations

35

References

2023

Year

Janine Reurink, Nicole Weisschuh, Alejandro Garanto, Adrian Dockery, L. Ingeborgh van den Born, Isabelle Fajardy, Lonneke Haer‐Wigman, Susanne Kohl, Bernd Wissinger, G. Jane Farrar,

Human Genetics and Genomics Advances

References

	Year	Citations

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