Hypoparathyroidism, deafness and renal dysplasia syndrome caused by a GATA3 splice site mutation leading to the activation of a cryptic splice site

por Gonçalves, Catarina I., Carriço, Josianne N., Omar, Omneya M., Abdalla, Ebtesam, Lemos, Manuel C.
Publicado 2023

Postnatal Sox6 Regulates Synaptic Function of Cortical Parvalbumin-Expressing Neurons

por Munguba, Hermany, Chattopadhyaya, Bidisha, Nilsson, Stephan, Carriço, Josianne N., Memic, Fatima, Oberst, Polina, Batista-Brito, Renata, Muñoz-Manchado, Ana Belen, Wegner, Michael, Fishell, Gordon, Di Cristo, Graziella, Hjerling-Leffler, Jens
Publicado 2021