PLXNB1 mutations in the etiology of idiopathic hypogonadotropic hypogonadism.
J Neuroendocrinol
; 34(4): e13103, 2022 04.
Article
in En
| MEDLINE
| ID: mdl-35170806
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Kallmann Syndrome
/
Receptors, Cell Surface
/
Hypogonadism
/
Nerve Tissue Proteins
Type of study:
Etiology_studies
/
Prognostic_studies
Limits:
Animals
/
Female
/
Humans
/
Male
Language:
En
Journal:
J Neuroendocrinol
Journal subject:
ENDOCRINOLOGIA
/
NEUROLOGIA
Year:
2022
Document type:
Article
Affiliation country:
Estados Unidos
Country of publication:
Estados Unidos