Omneya Magdy Omar
AuthID: R-00K-CPB
1
TITLE: Hypoparathyroidism, deafness and renal dysplasia syndrome caused by a GATA3 splice site mutation leading to the activation of a cryptic splice site Full Text
AUTHORS: Goncalves, Catarina I. I.; Carrico, Josianne N. N.; Omar, Omneya M. M.; Abdalla, Ebtesam; Lemos, Manuel C. C.;
PUBLISHED: 2023, SOURCE: FRONTIERS IN ENDOCRINOLOGY, VOLUME: 14
AUTHORS: Goncalves, Catarina I. I.; Carrico, Josianne N. N.; Omar, Omneya M. M.; Abdalla, Ebtesam; Lemos, Manuel C. C.;
PUBLISHED: 2023, SOURCE: FRONTIERS IN ENDOCRINOLOGY, VOLUME: 14
INDEXED IN: 
WOS
WOS2
TITLE: Clinically Relevant KCNQ1 Variants Causing KCNQ1-KCNE2 Gain-of-Function Affect the Ca2+ Sensitivity of the Channel Full Text
AUTHORS: Bauer, Christiane K.; Holling, Tess; Horn, Denise; Laco, Mario Noro; Abdalla, Ebtesam; Omar, Omneya Magdy; Alawi, Malik; Kutsche, Kerstin;
PUBLISHED: 2022, SOURCE: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, VOLUME: 23, ISSUE: 17
AUTHORS: Bauer, Christiane K.; Holling, Tess; Horn, Denise; Laco, Mario Noro; Abdalla, Ebtesam; Omar, Omneya Magdy; Alawi, Malik; Kutsche, Kerstin;
PUBLISHED: 2022, SOURCE: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, VOLUME: 23, ISSUE: 17
INDEXED IN: 
Scopus WOS
Scopus WOS