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
Document Type
Article
Year published
2025
Published
in JIMD REPORTS, ISSN: 2192-8312
Volume: 66, Issue: 3
Indexing
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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