Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency (Q28138497)
scientific article (publication date: April 1999)
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(P31) (Q13442814)
(P50) (Q37839560)
(Q40198131)
(P304) 655-660
(P407) (Q1860)
(P433) 4
(P478) 8
(P577) Thursday, April 1, 1999
(P1433) (Q2720965)
(P1476) "Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency" (language: en)
(P2093) V Ganapathy
X Wu
P Seth
P M Yuen
R J Wanders
T F Fok
N M Hjelm
(P2860) (Q40304719)
(Q36885831)
(Q24539033)
(Q24322836)
(Q24318913)
(Q41748291)
(Q28568689)
(Q42634050)
(Q28570027)
(Q24319690)
(Q48038909)
(Q59313590)
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description scientific article (publication date: April 1999)

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