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SCAGLIA, FERNANDO
One or more keywords matched the following items that are connected to
SCAGLIA, FERNANDO
Item Type
Name
Academic Article
Functional characterization of the carnitine transporter defective in primary carnitine deficiency.
Academic Article
Maternal systemic primary carnitine deficiency uncovered by newborn screening: clinical, biochemical, and molecular aspects.
Academic Article
Molecular spectrum of SLC22A5 (OCTN2) gene mutations detected in 143 subjects evaluated for systemic carnitine deficiency.
Concept
Organic Cation Transport Proteins
Search Criteria
Organic Cation Transport Proteins