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Encephalopathy Due to Defective Mitochondrial and Peroxisomal Fission 1
A syndrome that is caused by heterozygous mutation in the DNM1L gene, and is characterized by delayed psychomotor development and causes hypotonia that may lead to death in childhood.
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Overview
A syndrome that is caused by heterozygous mutation in the DNM1L gene, and is characterized by delayed psychomotor development and causes hypotonia that may lead to death in childhood.
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