Feichtinger, R.G.; Preisel, M.; Steinbrücker, K.; Brugger, K.; Radda, A.; Wortmann, S.B.; Mayr, J.A.
A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome. Genes 2022, 13, 2191.
https://doi.org/10.3390/genes13122191
AMA Style
Feichtinger RG, Preisel M, Steinbrücker K, Brugger K, Radda A, Wortmann SB, Mayr JA.
A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome. Genes. 2022; 13(12):2191.
https://doi.org/10.3390/genes13122191
Chicago/Turabian Style
Feichtinger, René G., Martin Preisel, Katja Steinbrücker, Karin Brugger, Alexandra Radda, Saskia B. Wortmann, and Johannes A. Mayr.
2022. "A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome" Genes 13, no. 12: 2191.
https://doi.org/10.3390/genes13122191
APA Style
Feichtinger, R. G., Preisel, M., Steinbrücker, K., Brugger, K., Radda, A., Wortmann, S. B., & Mayr, J. A.
(2022). A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome. Genes, 13(12), 2191.
https://doi.org/10.3390/genes13122191