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

AuthID
P-00W-F20
8
Author(s)
Fadiga, L
·
Lavrador, M
·
Barros, L
·
Al-Naama, A
·
Saraiva, LR
·
Document Type
Article
Year published
2022
Published
in INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, ISSN: 1661-6596
Volume: 23, Issue: 8
Indexing
Publication Identifiers
Pubmed: 35457241
Scopus: 2-s2.0-85128356501
Wos: WOS:000786027400001
Source Identifiers
ISSN: 1661-6596
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