Schüle, I.; Berger, U.; Matysiak, U.; Ruzaike, G.; Stiller, B.; Pohl, M.; Spiekerkoetter, U.; Lausch, E.; Grünert, S.C.; 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, 879.
https://doi.org/10.3390/genes12060879
AMA Style
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
Chicago/Turabian Style
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
APA Style
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