Title : Identification of DPAGT1 as a new gene in which mutations cause a congenital myasthenic syndrome - Belaya_2012_Ann.N.Y.Acad.Sci_1275_29 |
Author(s) : Belaya K , Finlayson S , Cossins J , Liu WW , Maxwell S , Palace J , Beeson D |
Ref : Annals of the New York Academy of Sciences , 1275 :29 , 2012 |
Abstract : Belaya_2012_Ann.N.Y.Acad.Sci_1275_29 |
ESTHER : Belaya_2012_Ann.N.Y.Acad.Sci_1275_29 |
PubMedSearch : Belaya_2012_Ann.N.Y.Acad.Sci_1275_29 |
PubMedID: 23278575 |
Belaya K, Finlayson S, Cossins J, Liu WW, Maxwell S, Palace J, Beeson D (2012)
Identification of DPAGT1 as a new gene in which mutations cause a congenital myasthenic syndrome
Annals of the New York Academy of Sciences
1275 :29
Belaya K, Finlayson S, Cossins J, Liu WW, Maxwell S, Palace J, Beeson D (2012)
Annals of the New York Academy of Sciences
1275 :29