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HARVARD Citation
Beaman, G. et al. (2019). A homozygous missense variant in CHRM3 associated with familial urinary bladder disease. Clinical genetics. 96 (6), pp. 515-520. [Online].
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Beaman, G. et al. (2019). A homozygous missense variant in CHRM3 associated with familial urinary bladder disease. Clinical genetics. 96 (6), pp. 515-520. [Online].