ArticleClinical genetics2019
A homozygous missense variant in CHRM3 associated with familial urinary bladder disease.
Glenda M Beaman et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
7 papers cite it
this papercites it
ArticleClinical genetics2019
Glenda M Beaman et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.