Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome.
Weber, Stefanie
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome. [electronic resource] - American journal of human genetics Nov 2011 - 668-74 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
1537-6605
10.1016/j.ajhg.2011.10.007 doi
Animals
Base Sequence
Consanguinity
Female
Frameshift Mutation--genetics
Humans
INDEL Mutation--genetics
Immunohistochemistry
Male
Metabolism, Inborn Errors--genetics
Mice
Mice, Knockout
Models, Molecular
Prune Belly Syndrome--genetics
Receptor, Muscarinic M3--deficiency
Sequence Homology, Nucleic Acid
Sex Factors
Urinary Bladder--embryology
Urinary Bladder Neck Obstruction--genetics
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome. [electronic resource] - American journal of human genetics Nov 2011 - 668-74 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
1537-6605
10.1016/j.ajhg.2011.10.007 doi
Animals
Base Sequence
Consanguinity
Female
Frameshift Mutation--genetics
Humans
INDEL Mutation--genetics
Immunohistochemistry
Male
Metabolism, Inborn Errors--genetics
Mice
Mice, Knockout
Models, Molecular
Prune Belly Syndrome--genetics
Receptor, Muscarinic M3--deficiency
Sequence Homology, Nucleic Acid
Sex Factors
Urinary Bladder--embryology
Urinary Bladder Neck Obstruction--genetics