A homozygous missense variant in CHRM3 associated with familial urinary bladder disease-Reference-Cited by-同舟云学术

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

Published:2019-09-11 Issue:6 Volume:96 Page:515-520
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Beaman Glenda M.¹²^ORCID,Galatà Gabriella¹²,Teik Keng W.³,Urquhart Jill E.¹²,Aishah Ali³,O'Sullivan James¹²,Bhaskar Sanjeev S.¹²,Wood Katherine A.¹²,Thomas Huw B.²,O'Keefe Raymond T.²,Woolf Adrian S.⁴⁵,Stuart Helen M.¹²,Newman William G.¹²⁶^ORCID

Affiliation:

1. Manchester Centre for Genomic MedicineManchester University NHS Foundation Trust, Health Innovation Manchester Manchester UK

2. Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human SciencesUniversity of Manchester Manchester UK

3. Department of GeneticsHospital Kuala Lumpur Kuala Lumpur Malaysia

4. Division of Cell Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology Medicine and HealthUniversity of Manchester, Manchester UK

5. Royal Manchester Children's HospitalManchester University NHS Foundation Trust, Manchester Academic Health Science Centre Manchester UK

6. Peking University Health Sciences Center Beijing China

Funder

Academy of Medical Sciences

Medical Research Council Canada

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13631

Reference22 articles.