TY  - GEN
AU  - van Maldegem,B T
AU  - Waterham,H R
AU  - Duran,M
AU  - van der Vlies,M
AU  - van Woerden,C S
AU  - Bobu,L L
AU  - Wanders,R J A
AU  - Wijburg,F A
TI  - The 625G>A SCAD gene variant is common but not associated with increased C4-carnitine in newborn blood spots
SN  - 0141-8955
PY  - 2005///0915
KW  - Alleles
KW  - Butyryl-CoA Dehydrogenase
KW  - deficiency
KW  - Carnitine
KW  - blood
KW  - Fatty Acids
KW  - metabolism
KW  - Genetic Predisposition to Disease
KW  - Genetic Variation
KW  - Heterozygote
KW  - Homozygote
KW  - Humans
KW  - Infant, Newborn
KW  - Lipid Metabolism, Inborn Errors
KW  - Neonatal Screening
KW  - Oxygen
KW  - Polymorphism, Genetic
KW  - Polymorphism, Restriction Fragment Length
KW  - Time Factors
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1007/s10545-005-0557-0
ER  -