| Title : Voluntary partial retraction of: Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes - |
| Author(s) : Croxen R , Hatton C , Shelley C , Brydson M , Chauplannaz G , Oosterhuis H , Vincent A , Newsom-Davis J , Colquhoun D , Beeson D |
| Ref : Neurology , 72 :294 , 2009 |
| PubMedID: 19153382 |
| Title : A human congenital myasthenia-causing mutation (epsilon L78P) of the muscle nicotinic acetylcholine receptor with unusual single channel properties - Shelley_2005_J.Physiol_564_377 |
| Author(s) : Shelley C , Colquhoun D |
| Ref : Journal of Physiology , 564 :377 , 2005 |
| Abstract : Shelley_2005_J.Physiol_564_377 |
| ESTHER : Shelley_2005_J.Physiol_564_377 |
| PubMedSearch : Shelley_2005_J.Physiol_564_377 |
| PubMedID: 15731194 |
| Title : Properties of the human muscle nicotinic receptor, and of the slow-channel myasthenic syndrome mutant epsilonL221F, inferred from maximum likelihood fits - Hatton_2003_J.Physiol_547_729 |
| Author(s) : Hatton CJ , Shelley C , Brydson M , Beeson D , Colquhoun D |
| Ref : Journal of Physiology , 547 :729 , 2003 |
| Abstract : Hatton_2003_J.Physiol_547_729 |
| ESTHER : Hatton_2003_J.Physiol_547_729 |
| PubMedSearch : Hatton_2003_J.Physiol_547_729 |
| PubMedID: 12562900 |
| Title : Structural abnormalities of the AChR caused by mutations underlying congenital myasthenic syndromes - Beeson_2003_Ann.N.Y.Acad.Sci_998_114 |
| Author(s) : Beeson D , Webster R , Ealing J , Croxen R , Brownlow S , Brydson M , Newsom-Davis J , Slater CR , Hatton C , Shelley C , Colquhoun D , Vincent A |
| Ref : Annals of the New York Academy of Sciences , 998 :114 , 2003 |
| Abstract : Beeson_2003_Ann.N.Y.Acad.Sci_998_114 |
| ESTHER : Beeson_2003_Ann.N.Y.Acad.Sci_998_114 |
| PubMedSearch : Beeson_2003_Ann.N.Y.Acad.Sci_998_114 |
| PubMedID: 14592868 |
| Title : Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes - Croxen_2002_Neurology_59_162 |
| Author(s) : Croxen R , Hatton C , Shelley C , Brydson M , Chauplannaz G , Oosterhuis H , Vincent A , Newsom-Davis J , Colquhoun D , Beeson D |
| Ref : Neurology , 59 :162 , 2002 |
| Abstract : Croxen_2002_Neurology_59_162 |
| ESTHER : Croxen_2002_Neurology_59_162 |
| PubMedSearch : Croxen_2002_Neurology_59_162 |
| PubMedID: 12141316 |