Severe congenital cutis laxa: Identification of novel homozygous LOX gene variants in two families.
Clin Genet
; 100(2): 168-175, 2021 08.
Article
in En
| MEDLINE
| ID: mdl-33866545
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Abnormalities, Multiple
/
Cutis Laxa
/
Protein-Lysine 6-Oxidase
Type of study:
Diagnostic_studies
/
Etiology_studies
/
Prognostic_studies
Limits:
Adult
/
Female
/
Humans
/
Male
/
Pregnancy
Language:
En
Journal:
Clin Genet
Year:
2021
Document type:
Article
Affiliation country:
Australia
Country of publication:
Denmark