Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome. [electronic resource]
Producer: 20120221Description: 668-74 p. digitalISSN:- 1537-6605
- 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
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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