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 S epsilon RAC1
Sarig, O, Goldsher, D, Nousbeck, J, Fuchs-Telem, D, Cohen-Katsenelson, K, Iancu, T C, Manov, I, Saada, A, Sprecher, E, Mandel, H
Published in American journal of medical genetics. Part A (01.09.2013)
Published in American journal of medical genetics. Part A (01.09.2013)
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