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Journal: Genes, 2022
Volume: 13
Number: 2191

Article: A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome
Authors: by René G. Feichtinger, Martin Preisel, Katja Steinbrücker, Karin Brugger, Alexandra Radda, Saskia B. Wortmann and Johannes A. Mayr
Link: https://www.mdpi.com/2073-4425/13/12/2191

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