Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Laura Calvo López"'
Publikováno v:
HemaSphere, Vol 7, p e532625e (2023)
Externí odkaz:
https://doaj.org/article/970f9c395eaa45d9bac3be1afa35b993
Autor:
Izarbe Aísa-Marín, Quirze Rovira, Noelia Díaz, Laura Calvo-López, Juan M. Vaquerizas, Gemma Marfany
Publikováno v:
Neurobiology of Disease, Vol 194, Iss , Pp 106463- (2024)
Mutations in NR2E3, a gene encoding an orphan nuclear transcription factor, cause two retinal dystrophies with a distinct phenotype, but the precise role of NR2E3 in rod and cone transcriptional networks remains unclear. To dissect NR2E3 function, we
Externí odkaz:
https://doaj.org/article/4b20d1218f04487b9cb26700edb5e32e