A Novel Fgfr1 Missense Mutation in a Portuguese Family with Congenital Hypogonadotropic Hypogonadism

AuthID
 P-00W-F20
8
Author(s)
Fadiga, L
·
Lavrador, M
·
Vicente, N
·
Barros, L
·
Goncalves, CI
·
Al-Naama, A
·
Saraiva, LR
·
Tipo de Documento
Article
Year published
2022
Publicado
in INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, ISSN: 16616596
Volume: 23, Número: 8, Páginas: 4423 (7)
Indexing
Wos®
Scopus®
Crossref®1
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 35457241
SCOPUS: 2-s2.0-85128356501
Wos: WOS:000786027400001
Source Identifiers
ISSN: 16616596
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