(Q22010737)
Statements
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene (English)
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1 reference
2 references
L C Papadopoulou
1 reference
C M Sue
1 reference
M M Davidson
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K Tanji
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J E Sadlock
1 reference
S Krishna
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W Walker
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J Selby
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D M Glerum
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R V Coster
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G Lyon
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E Scalais
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R Lebel
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P Kaplan
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S Shanske
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D C De Vivo
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E Bonilla
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S DiMauro
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E A Schon
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November 1999
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23
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3
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333-7
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