Atypical Megdhel Syndrome: A Milder Phenotype With Hepatic Presentation and Failure to Thrive Associated With a Homozygous Nonsense Variant of Serac1

AuthID
 P-018-T55
6
Author(s)
Pita, RM
·
Gonçalves, I
·
Nobre, S
Tipo de Documento
Article
Year published
2025
Publicado
in JIMD REPORTS, ISSN: 2192-8312
Volume: 66, Número: 3
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Wos®
Scopus®
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 40365324
SCOPUS: 2-s2.0-105004760804
Wos: WOS:001578943900001
Source Identifiers
ISSN: 2192-8312
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