Intragenic Deletions in Nrxn1: Insights from Acgh Analysis in Neurodevelopmental Disorders

AuthID
 P-018-DFV
6
Author(s)
Pinto, J
·
Almeida, C
·
Pinho, MJ
·
Santos, MH
·
Grangeia, A
Tipo de Documento
Abstract
Year published
2024
Publicado
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 32, Páginas: 1584-1585 (2)
Indexing
Wos®
Publication Identifiers
Wos: WOS:001407868902507
Source Identifiers
ISSN: 1018-4813
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