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Author
Alibakhshi R
Alibakhshi R
References (2)
1. MDGA2 homozygous loss-of-function variants cause developmental and epileptic encephalopathy - Morsy_2026_Am.J.Hum.Genet__
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 :
View Abstract
PubMedSearch :
Morsy_2026_Am.J.Hum.Genet__
PubMedID
:
41570816
2. Association between activity and genotypes of paraoxonase1 L55M (rs854560) increases the disease activity of rheumatoid arthritis through oxidative stress - Tanhapour_2019_Mol.Biol.Rep_46_741
Title :
Association between activity and genotypes of paraoxonase1 L55M (rs854560) increases the disease activity of rheumatoid arthritis through oxidative stress -
Tanhapour_2019_Mol.Biol.Rep_46_741
Author(s) :
Tanhapour M
,
Shahmohamadnejad S
,
Vaisi-Raygani A
,
Kiani A
,
Shakiba Y
,
Rahimi Z
,
Bahrehmand F
,
Shakiba E
,
Vaisi-Raygani AA
,
Alibakhshi R
,
Eivazi A
,
Pourmotabbed T
Ref :
Mol Biol Rep ,
46
:741 , 2019
Abstract :
View Abstract
PubMedSearch :
Tanhapour_2019_Mol.Biol.Rep_46_741
PubMedID
:
30506510