Jang G

References (2)

Title : MDGA2 homozygous loss-of-function variants cause developmental and epileptic encephalopathy - Morsy_2026_Am.J.Hum.Genet__
Author(s) : Morsy H , Kim H , Jang G , Zaki MS , Severino M , Abdelrazek IM , Hussien H , Self E , Albaradie RS , Bakur K , Firoozfar Z , Efthymiou S , Noureldeen MM , Nabil A , Alvi JR , Molavi F , Alavi S , Alibakhshi R , Topcu V , Mancilar H , Uctepe E , Yesilyurt A , Aldhalaan H , Showki Tous ES , Alhaddad B , Elbendary HM , Scardamaglia A , Murphy D , Yepez VA , Gagneur J , Omar TI , Abd Elmaksoud M , Vandrovocova J , Abdalla E , Reilly MM , Sultan T , Alkuraya FS , Gleeson JG , Um JW , Houlden H , Ko J , Maroofian R
Ref : American Journal of Human Genetics , : , 2026
Abstract :
PubMedSearch : Morsy_2026_Am.J.Hum.Genet__
PubMedID: 41570816

Title : MDGAs perform activity-dependent synapse type-specific suppression via distinct extracellular mechanisms - Kim_2024_Proc.Natl.Acad.Sci.U.S.A_121_e2322978121
Author(s) : Kim S , Jang G , Kim H , Lim D , Han KA , Um JW , Ko J
Ref : Proc Natl Acad Sci U S A , 121 :e2322978121 , 2024
Abstract :
PubMedSearch : Kim_2024_Proc.Natl.Acad.Sci.U.S.A_121_e2322978121
PubMedID: 38900791