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

CHRM3 codes for the M3 muscarinic acetylcholine receptor that is located on the surface of smooth muscle cells of the detrusor, the muscle that effects urinary voiding. Previously, we reported brothers in a family affected by a congenital prune belly‐like syndrome with mydriasis due to homozygous CH...

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Detalles Bibliográficos
Autores principales: Beaman, Glenda M., Galatà, Gabriella, Teik, Keng W., Urquhart, Jill E., Aishah, Ali, O'Sullivan, James, Bhaskar, Sanjeev S., Wood, Katherine A., Thomas, Huw B., O'Keefe, Raymond T., Woolf, Adrian S., Stuart, Helen M., Newman, William G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899476/
https://www.ncbi.nlm.nih.gov/pubmed/31441039
http://dx.doi.org/10.1111/cge.13631

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899476/
https://www.ncbi.nlm.nih.gov/pubmed/31441039
http://dx.doi.org/10.1111/cge.13631

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