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Luo, S. et al. (2022). A novel variant in the HX repeat motif of ATN1 in a Chinese patient with CHEDDA syndrome and literature review. Molecular genetics & genomic medicine. 10 (12), p. n/a. [Online].
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Luo, S. et al. (2022). A novel variant in the HX repeat motif of ATN1 in a Chinese patient with CHEDDA syndrome and literature review. Molecular genetics & genomic medicine. 10 (12), p. n/a. [Online].