Neonatal mitochondrial hepatoencephalopathy caused by novel GFM1 mutations.

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Published in Mol Genet Metab Rep on February 20, 2015

Authors

Kirstine Ravn1, Bitten Schönewolf-Greulich2, Rikke M Hansen3, Anna-Helene Bohr4, Morten Duno1, Flemming Wibrand1, Elsebet Ostergaard1

Author Affiliations

1: Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Blegdamsvej 9, Copenhagen, Denmark.
2: Department of Clinical Genetics, Kennedy Center, Copenhagen University Hospital, Rigshospitalet, Glostrup, Denmark.
3: Pediatrics Department, Herning Hospital, Herning, Denmark.
4: Pediatrics Department, Nykoebing Falster Hospital, Nykoebing Falster, Denmark.

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