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Schüle I, Berger U, Matysiak U, Ruzaike G, Stiller B, Pohl M, Spiekerkoetter U, Lausch E, Grünert SC, Schmidts M. A Homozygous Deletion of Exon 5 of KYNU Resulting from a Maternal Chromosome 2 Isodisomy (UPD2) Causes Catel-Manzke-Syndrome/VCRL Syndrome. Genes. 2021; 12(6):879. https://doi.org/10.3390/genes12060879

Schüle, Isabel, Urs Berger, Uta Matysiak, Gunda Ruzaike, Brigitte Stiller, Martin Pohl, Ute Spiekerkoetter, Ekkehart Lausch, Sarah C. Grünert, and Miriam Schmidts. 2021. "A Homozygous Deletion of Exon 5 of KYNU Resulting from a Maternal Chromosome 2 Isodisomy (UPD2) Causes Catel-Manzke-Syndrome/VCRL Syndrome" Genes 12, no. 6: 879. https://doi.org/10.3390/genes12060879

Schüle, I., Berger, U., Matysiak, U., Ruzaike, G., Stiller, B., Pohl, M., Spiekerkoetter, U., Lausch, E., Grünert, S. C., & Schmidts, M. (2021). A Homozygous Deletion of Exon 5 of KYNU Resulting from a Maternal Chromosome 2 Isodisomy (UPD2) Causes Catel-Manzke-Syndrome/VCRL Syndrome. Genes, 12(6), 879. https://doi.org/10.3390/genes12060879