Familial Pulmonary Fibrosis with Dyskeratosis Congenita Associated with a Rare Rtel1 Gene Mutation

AuthID
 P-018-JGB
3
Author(s)
Cortesao, C
·
Balanco, L
·
Tipo de Documento
Article
Year published
2025
Publicado
in BMJ CASE REPORTS, ISSN: 1757-790X
Volume: 18, Número: 4
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Publication Identifiers
Pubmed: 40199602
SCOPUS: 2-s2.0-105002385915
Wos: WOS:001463146200001
Source Identifiers
ISSN: 1757-790X
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