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HARVARD Citation
Woimant, F. et al. (2020). A novel deep intronic variant in ATP7B in five unrelated families affected by Wilson disease. Molecular genetics & genomic medicine. 8 (10), p. n/a. [Online].
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Woimant, F. et al. (2020). A novel deep intronic variant in ATP7B in five unrelated families affected by Wilson disease. Molecular genetics & genomic medicine. 8 (10), p. n/a. [Online].