Severe Kidar Syndrome Caused by Deletion in the Ap1B1 Gene: Report of a Teenage Patient and Systematic Review of the Literature

AuthID
P-00Z-0MB
8
Author(s)
Nogueira, A
·
Matos, P
·
Pinto, J
·
Tipo de Documento
Review
Year published
2023
Publicado
in EUROPEAN JOURNAL OF MEDICAL GENETICS, ISSN: 1769-7212
Volume: 66, Número: 10, Páginas: 104827 (6)
Indexing
Publication Identifiers
Pubmed: 37657632
SCOPUS: 2-s2.0-85170248894
Wos: WOS:001081562900001
Source Identifiers
ISSN: 1769-7212
Export Publication Metadata
Info
At this moment we don't have any links to full text documens.