APA (7th ed.) Citation

A, B., C, V., C, N., E, T., AT, T., F, B., . . . HJ, B. (2026). An example for potentially underrated causes of recessive disease in the Greater Middle East: Integrative long-read genome and transcriptome sequencing pinpoint a deep-intronic homozygous HEXB candidate founder variant in GM2-gangliosidosis. Human genomics, 20(1), . https://doi.org/10.1186/s40246-026-00995-y

Chicago Style (17th ed.) Citation

A, Bolte, Velmans C, Netzer C, Thimm E, Tuncel AT, Bürger F, Hiersche M, Betz C, and Bolz HJ. "An Example for Potentially Underrated Causes of Recessive Disease in the Greater Middle East: Integrative Long-read Genome and Transcriptome Sequencing Pinpoint a Deep-intronic Homozygous HEXB Candidate Founder Variant in GM2-gangliosidosis." Human Genomics 20, no. 1 (2026). https://doi.org/10.1186/s40246-026-00995-y.

MLA (9th ed.) Citation

A, Bolte, et al. "An Example for Potentially Underrated Causes of Recessive Disease in the Greater Middle East: Integrative Long-read Genome and Transcriptome Sequencing Pinpoint a Deep-intronic Homozygous HEXB Candidate Founder Variant in GM2-gangliosidosis." Human Genomics, vol. 20, no. 1, 2026, https://doi.org/10.1186/s40246-026-00995-y.