A Serious and Unusual Presentation of Congenital Isolated Acth Deficiency Due to Tbx19 Mutation, Beyond the Neonatal Period

AuthID
 P-00X-9VA
9
Author(s)
Vieira, IH
·
Bala, NM
·
Dinis, I
·
Cardoso, R
·
Paiva, I
·
Mirante, A
Tipo de Documento
Article
Year published
2022
Publicado
in ENDOCRINOLOGY DIABETES AND METABOLISM CASE REPORTS
Volume: 2022, Número: 1
Indexing
Wos®
Scopus®
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 36070412
SCOPUS: 2-s2.0-85139011479
Wos: WOS:000869538400001
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