Long term follow-up in two siblings with Sengers syndrome: Case report
Abstract Background Sengers syndrome is characterized by congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy, and lactic acidosis associated with mutations in AGK gene. Clinical course ranges from a severe fatal neonatal form, to a more benign form allowing survival into adultho...
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Main Authors: | , , , , , , , , , , |
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Format: | Book |
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BMC,
2022-10-01T00:00:00Z.
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