Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene (Q22010737)
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(P31) (Q13442814)
(P50) (Q37828689)
(Q89906306)
(P304) 333-7
(P407) (Q1860)
(P433) 3
(P478) 23
(P577) +1999-11-00T00:00:00Z
(P1433) (Q976454)
(P1476) "Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene" (language: en)
(P2093) L C Papadopoulou
C M Sue
M M Davidson
K Tanji
J E Sadlock
S Krishna
W Walker
J Selby
D M Glerum
R V Coster
G Lyon
E Scalais
R Lebel
P Kaplan
S Shanske
D C De Vivo
E Bonilla
S DiMauro
E A Schon
(P2860) (Q47910949)
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(Q22008622)
(Q24323240)
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(Q70167731)
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(Q33681493)
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(Q27939251)
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(Q34450341)
(Q68486954)
(Q71246164)
(Q27934782)
(Q74609082)
(Q48203324)
(Q44771353)
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(Q71890063)
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