A Novel SEMA3G Mutation in Two Siblings Affected by Syndromic GnRH Deficiency.
Neuroendocrinology
; 111(5): 421-441, 2021.
Article
in En
| MEDLINE
| ID: mdl-32365351
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Gonadotropin-Releasing Hormone
/
Semaphorins
/
Hypogonadism
/
Hypothalamo-Hypophyseal System
Type of study:
Etiology_studies
/
Prognostic_studies
Limits:
Animals
/
Humans
/
Male
Language:
En
Journal:
Neuroendocrinology
Year:
2021
Document type:
Article
Affiliation country:
Italy
Country of publication:
Switzerland