Two novel missense mutations of the OCTN2 gene (W283R and V446F) in a patient with primary systemic carnitine deficiency (Q28141397)
scientific article (publication date: 2000)
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Current Data About Two novel missense mutations of the OCTN2 gene (W283R and V446F) in a patient with primary systemic carnitine deficiency
(P31) (Q13442814)

(P304) 118

(P407) (Q1860)

(P433) 1

(P478) 15

(P577) +2000-01-00T00:00:00Z

(P921) (Q181600)
(P887)

(P1433) (Q5937269)

(P1476) "Two novel missense mutations of the OCTN2 gene (W283R and V446F) in a patient with primary systemic carnitine deficiency" (language: en)

(P2093) E Mayatepek
(P1545) 1

J Nezu
(P1545) 2

I Tamai
(P1545) 3

A Oku
(P1545) 4

M Katsura
(P1545) 5

M Shimane
(P1545) 6

A Tsuji
(P1545) 7

other details
description scientific article (publication date: 2000)

External Links
(P356) 10.1002/(SICI)1098-1004(200001)15:1<118::AID-HUMU28>3.0.CO;2-8
(P698) 10612840