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
·
Tipo de Documento
Review
Year published
2023
Publicado
in EUROPEAN JOURNAL OF MEDICAL GENETICS, ISSN: 1769-7212
Volume: 66, Número: 10, Páginas: 104827 (6)
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Pubmed®
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Publication Identifiers
Pubmed: 37657632
SCOPUS: 2-s2.0-85170248894
Wos: WOS:001081562900001
Source Identifiers
ISSN: 1769-7212
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