Carnitine transporter OCTN2 mutations in systemic primary carnitine deficiency: a novel Arg169Gln mutation and a recurrent Arg282ter mutation associated with an unconventional splicing abnormality (Q28140684)
scientific article (publication date: 2 August 1999)
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Current Data About Carnitine transporter OCTN2 mutations in systemic primary carnitine deficiency: a novel Arg169Gln mutation and a recurrent Arg282ter mutation associated with an unconventional splicing abnormality
(P31) (Q13442814)

(P304) 484-7

(P407) (Q1860)

(P433) 2

(P478) 261

(P577) Monday, August 2, 1999

(P921) (Q3358135)

(P1433) (Q864228)

(P1476) "Carnitine transporter OCTN2 mutations in systemic primary carnitine deficiency: a novel Arg169Gln mutation and a recurrent Arg282ter mutation associated with an unconventional splicing abnormality" (language: en)

(P2093) B Burwinkel
(P1545) 1

J Kreuder
(P1545) 2

S Schweitzer
(P1545) 3

M Vorgerd
(P1545) 4

K Gempel
(P1545) 5

K D Gerbitz
(P1545) 6

M W Kilimann
(P1545) 7

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description scientific article (publication date: 2 August 1999)

External Links
(P356) 10.1006/BBRC.1999.1060
(P698) 10425211