HIGHLIGHTS
- who: Katarzyna Gaweda-Walerych and colleagues from the Department of Neurogenetics and Functional Genomics, Mossakowski Medical Research Institute, Polish Academy of Sciences, Warsaw, Poland and Psychiatric Nursing, Faculty of Health Sciences, Medical University of Gdansk, Gdansk, Poland have published the research work: A Patient with Corticobasal Syndrome and Progressive Non-Fluent Aphasia (CBS-PNFA), with Variants in ATP7B, SETX, SORL1, and FOXP1 Genes, in the Journal: Genes 2022, 2361 of /2022/
- what: The authors focused on the rare variants with the highest putative impact on the disease phenotype . The authors provide evidence of an altered . . .
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