FERNANDO SCAGLIA to Solute Carrier Family 22 Member 5
This is a "connection" page, showing publications FERNANDO SCAGLIA has written about Solute Carrier Family 22 Member 5.
Connection Strength
0.082
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Functional characterization of the carnitine transporter defective in primary carnitine deficiency. Arch Biochem Biophys. 1999 Apr 01; 364(1):99-106.
Score: 0.039
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Molecular spectrum of SLC22A5 (OCTN2) gene mutations detected in 143 subjects evaluated for systemic carnitine deficiency. Hum Mutat. 2010 Aug; 31(8):E1632-51.
Score: 0.022
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Maternal systemic primary carnitine deficiency uncovered by newborn screening: clinical, biochemical, and molecular aspects. Genet Med. 2010 Jan; 12(1):19-24.
Score: 0.021