APA (7th ed.) Citation

Neuhaus, C., & Rohrschneider, K. (2017). Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: Copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome. Molecular genetics & genomic medicine, 5(5), . https://doi.org/10.1002/mgg3.312

Chicago Style (17th ed.) Citation

Neuhaus, Christine, and Klaus Rohrschneider. "Next-generation Sequencing Reveals the Mutational Landscape of Clinically Diagnosed Usher Syndrome: Copy Number Variations, Phenocopies, a Predominant Target for Translational Read-through, and PEX26 Mutated in Heimler Syndrome." Molecular Genetics & Genomic Medicine 5, no. 5 (2017). https://doi.org/10.1002/mgg3.312.

MLA (9th ed.) Citation

Neuhaus, Christine, and Klaus Rohrschneider. "Next-generation Sequencing Reveals the Mutational Landscape of Clinically Diagnosed Usher Syndrome: Copy Number Variations, Phenocopies, a Predominant Target for Translational Read-through, and PEX26 Mutated in Heimler Syndrome." Molecular Genetics & Genomic Medicine, vol. 5, no. 5, 2017, https://doi.org/10.1002/mgg3.312.