A homozygous missense variant in CHRM3 associated with familial urinary bladder disease.

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Source: Clinical Genetics - August 22, 2019 Category: Genetics & Stem Cells Authors: Beaman GM, Galatà G, Keng WT, Urquhart JE, Aishah A, O'Sullivan J, Bhaskar SS, Wood KA, Thomas HB, O'Keefe RT, Woolf AS, Stuart HM, Newman WG Tags: Clin Genet Source Type: research