A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome.
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| Title: | A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome. |
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| Authors: | Feichtinger, René G.1 (AUTHOR), Preisel, Martin1 (AUTHOR), Steinbrücker, Katja1 (AUTHOR), Brugger, Karin1 (AUTHOR), Radda, Alexandra2 (AUTHOR), Wortmann, Saskia B.1,3 (AUTHOR) s.wortmann@salk.at, Mayr, Johannes A.1 (AUTHOR) |
| Source: | Genes. Dec2022, Vol. 13 Issue 12, p2191. 6p. |
| Database: | Academic Search Ultimate |
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| ISSN: | 20734425 |
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| DOI: | 10.3390/genes13122191 |
