Associated Papers
A homozygous missense variant in CHRM3 associated with familial urinary bladder disease.
Beaman GM et al.
Clinical Genetics, 2019
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome.
Weber S et al.
American Journal of Human Genetics, 2011
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