Hatton C

References (3)

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 : 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