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p(HGNC:SLC25A4) -| path(SDIS:Myopathy)
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Approximately 61,000 statements.
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Copyright (c) 2011-2012, Selventa. All rights reserved.
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BEL Framework Large Corpus Document
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More important as a cause of respiratory chain dysfunction is a de¢ciency of the adenine nucleotide translocator (ANT). This has been described in one child with mitochondrial myopathy, and has been attributed to a speci¢c defect of the muscle/heart subunit ANT1 [25]. The lack of cardiac symptoms in that child at age 8 is a little surprising, because a `knockout' mouse de¢cient in ANT1 showed not only mitochondrial myopathy but also hypertrophic cardiomyopathy with mitochondrial proliferation [26].
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Selventa
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