Cite
HARVARD Citation
Latchman, K. et al. (2020). A founder noncoding GALT variant interfering with splicing causes galactosemia. Journal of inherited metabolic disease. 43 (6), pp. 1199-1204. [Online].
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Latchman, K. et al. (2020). A founder noncoding GALT variant interfering with splicing causes galactosemia. Journal of inherited metabolic disease. 43 (6), pp. 1199-1204. [Online].