TY  - GEN
AU  - Weber,Stefanie
AU  - Thiele,Holger
AU  - Mir,Sevgi
AU  - Toliat,Mohammad Reza
AU  - Sozeri,Betül
AU  - Reutter,Heiko
AU  - Draaken,Markus
AU  - Ludwig,Michael
AU  - Altmüller,Janine
AU  - Frommolt,Peter
AU  - Stuart,Helen M
AU  - Ranjzad,Parisa
AU  - Hanley,Neil A
AU  - Jennings,Rachel
AU  - Newman,William G
AU  - Wilcox,Duncan T
AU  - Thiel,Uwe
AU  - Schlingmann,Karl Peter
AU  - Beetz,Rolf
AU  - Hoyer,Peter F
AU  - Konrad,Martin
AU  - Schaefer,Franz
AU  - Nürnberg,Peter
AU  - Woolf,Adrian S
TI  - Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome
SN  - 1537-6605
PY  - 2012///0221
KW  - Animals
KW  - Base Sequence
KW  - Consanguinity
KW  - Female
KW  - Frameshift Mutation
KW  - genetics
KW  - Humans
KW  - INDEL Mutation
KW  - Immunohistochemistry
KW  - Male
KW  - Metabolism, Inborn Errors
KW  - Mice
KW  - Mice, Knockout
KW  - Models, Molecular
KW  - Prune Belly Syndrome
KW  - Receptor, Muscarinic M3
KW  - deficiency
KW  - Sequence Homology, Nucleic Acid
KW  - Sex Factors
KW  - Urinary Bladder
KW  - embryology
KW  - Urinary Bladder Neck Obstruction
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.ajhg.2011.10.007
ER  -