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Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome.
Weber, Stefanie; Thiele, Holger; Mir, Sevgi; Toliat, Mohammad Reza; Sozeri, Betül; Reutter, Heiko; Draaken, Markus; Ludwig, Michael; Altmüller, Janine; Frommolt, Peter; Stuart, Helen M; Ranjzad, Parisa; Hanley, Neil A; Jennings, Rachel; Newman, William G; Wilcox, Duncan T; Thiel, Uwe; Schlingmann, Karl Peter; Beetz, Rolf; Hoyer, Peter F; Konrad, Martin; Schaefer, Franz; Nürnberg, Peter; Woolf, Adrian S.
Affiliation
  • Weber S; Pediatrics II, University Children's Hospital Essen, 45122 Essen, Germany. stefanie.weber@uk.essen.de
Am J Hum Genet ; 89(5): 668-74, 2011 Nov 11.
Article in En | MEDLINE | ID: mdl-22077972
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prune Belly Syndrome / Urinary Bladder / Receptor, Muscarinic M3 / Metabolism, Inborn Errors Type of study: Etiology_studies / Prognostic_studies Limits: Animals / Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 2011 Type: Article Affiliation country: Germany
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prune Belly Syndrome / Urinary Bladder / Receptor, Muscarinic M3 / Metabolism, Inborn Errors Type of study: Etiology_studies / Prognostic_studies Limits: Animals / Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 2011 Type: Article Affiliation country: Germany