Exploring The Missing Link Between Primary Cilia And Neurodevelopmental Disorders: The Case Of A Novel Mbd5 Variant In A Patient With Severe Epilepsy

AuthID
 P-00Y-TX7
15
Author(s)
Martins, M
·
RafaelaOliveira, A
·
Martins, S
·
Perdigao, P
·
Palma, P
·
Almeida, LP
·
Oliveira, G
·
Peca, J
·
Seabra, CM
Tipo de Documento
Abstract
Year published
2023
Publicado
in MEDICINE, ISSN: 0025-7974
Volume: 102, Número: 13
Conference
26Th Annual Meeting of the Portuguese-Society-Of-Human-Genetics (Spgh), Date: NOV 17-19, 2022, Location: Coimbra, PORTUGAL
Indexing
Wos®
Publication Identifiers
Wos: WOS:001005724900025
Source Identifiers
ISSN: 0025-7974
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