Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-Methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and leigh-Like Syndrome) caused by novel mutations in SERAC1
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| Description | scientific article published on 05 August 2013 |
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author: Irena Manov Ann Saada |
| Publication date | August 5, 2013 |
| Language | English |
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