Addendum to “Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiency” [Mol. Genet. Metab. 77 (2002) 195–201]

✍ Scribed by Stephen D. Cederbaum; Samantha Koo-McCoy; Ingrid Tein; Betty Y.L. Hsu; Arupa Ganguly; Eric Vilain; Katrina Dipple; Ljerka Cvitanovic-Sojat; Charles Stanley

• Book ID: 117735462
• Publisher: Elsevier Science
• Year: 2003
• Tongue: English
• Weight: 53 KB
• Volume: 78
• Category: Article
• ISSN: 1096-7192
• DOI: 10.1016/s1096-7192(02)00202-0