Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines.
J Inherit Metab Dis
; 38(6): 1007-19, 2015 Nov.
Article
in En
| MEDLINE
| ID: mdl-25762406
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Neonatal Screening
/
Methylenetetrahydrofolate Reductase (NADPH2)
/
Homocystinuria
Type of study:
Diagnostic_studies
/
Guideline
/
Screening_studies
/
Systematic_reviews
Limits:
Humans
/
Newborn
Language:
En
Journal:
J Inherit Metab Dis
Year:
2015
Document type:
Article
Affiliation country:
Suiza
Country of publication:
Estados Unidos