A case of homozygous familial hypercholesterolemia with an atypical phenotype and delayed clinical symptoms.
J Clin Lipidol
; 15(3): 435-440, 2021.
Article
in En
| MEDLINE
| ID: mdl-33975813
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Phenotype
/
Homozygote
/
Hyperlipoproteinemia Type II
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Female
/
Humans
/
Middle aged
Language:
En
Journal:
J Clin Lipidol
Journal subject:
BIOQUIMICA
/
METABOLISMO
Year:
2021
Document type:
Article