Whole exome sequencing reveals several novel variants in congenital disorders of glycosylation and glycogen storage diseases in seven patients from Iran.
Mol Genet Genomic Med
; 11(2): e2099, 2023 02.
Article
in En
| MEDLINE
| ID: mdl-36579437
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Glycogen Storage Disease
/
Congenital Disorders of Glycosylation
Limits:
Humans
Country/Region as subject:
Asia
Language:
En
Journal:
Mol Genet Genomic Med
Year:
2023
Document type:
Article
Affiliation country:
Irán