Prader-Willi Syndrome and PCSK1 mutation: a novel presentation of combined syndromic and monogenic obesity.
Eur Rev Med Pharmacol Sci
; 26(7): 2437-2442, 2022 04.
Article
in En
| MEDLINE
| ID: mdl-35442499
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Prader-Willi Syndrome
Type of study:
Diagnostic_studies
Limits:
Adult
/
Humans
/
Male
Language:
En
Journal:
Eur Rev Med Pharmacol Sci
Journal subject:
FARMACOLOGIA
/
TOXICOLOGIA
Year:
2022
Document type:
Article
Affiliation country:
Greece