| 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 : 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 : |
| 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 : |
| PubMedSearch : Croxen_2002_Neurology_59_162 |
| PubMedID: 12141316 |
| Title : End-plate gamma- and epsilon-subunit mRNA levels in AChR deficiency syndrome due to epsilon-subunit null mutations - Croxen_2001_Brain_124_1362 |
| Author(s) : Croxen R , Young C , Slater C , Haslam S , Brydson M , Vincent A , Beeson D |
| Ref : Brain , 124 :1362 , 2001 |
| Abstract : |
| PubMedSearch : Croxen_2001_Brain_124_1362 |
| PubMedID: 11408331 |
| Title : Genes at the junction--candidates for congenital myasthenic syndromes. - Vincent_1997_Trends.Neurosci_20_15 |
| Author(s) : Vincent A , Newland C , Croxen R , Beeson D |
| Ref : Trends in Neurosciences , 20 :15 , 1997 |
| Abstract : |
| PubMedSearch : Vincent_1997_Trends.Neurosci_20_15 |
| PubMedID: 9004414 |