TY  - JOUR
AU  - Mayo, Sonia
AU  - Gómez Manjón, Irene
AU  - Fernández Martínez, Fco. Javier
AU  - Camacho Salas, Ana
AU  - Martínez, Francisco
AU  - Benito León, Julián
PY  - 2021
DO  - 10.3390/ijms22115609
SN  - 1422-0067
UR  - https://hdl.handle.net/20.500.14352/7050
T2  - International Journal of Molecular Sciences
AB  - Eyelid myoclonia with absences (EMA), also known as Jeavons syndrome (JS) is a childhood onset epileptic syndrome with manifestations involving a clinical triad of absence seizures with eyelid myoclonia (EM), photosensitivity (PS), and seizures or...
LA  - eng
M2  - 5609
PB  - MPDI
KW  - Jeavons syndrome
KW  - eyelid myoclonia with absences
KW  - candidate genes
KW  - SYNGAP1
KW  - KIA02022
KW  - NEXMIF
KW  - RORB
KW  - CHD2
TI  - Candidate Genes for Eyelid Myoclonia with Absences, Review of the Literature
TY  - journal article
VL  - 22
ER  -