Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency (Q28140889)
scientific article (publication date: 22 March 2000)
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Current Data About Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency
(P31) (Q13442814)

(P304) 795-801

(P407) (Q1860)

(P433) 5

(P478) 9

(P577) Wednesday, March 22, 2000

(P921) (Q1364270)
(P887)

(P1433) (Q2720965)

(P1476) "Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency" (language: en)

(P2093) M Jaksch
(P1545) 1

I Ogilvie
(P1545) 2

J Yao
(P1545) 3

G Kortenhaus
(P1545) 4

H G Bresser
(P1545) 5

K D Gerbitz
(P1545) 6

E A Shoubridge
(P1545) 7

other details
description scientific article (publication date: 22 March 2000)

External Links
(P356) 10.1093/HMG/9.5.795
(P698) 10749987
(P5875) 279404875