Open Access Research article

Molecular and biochemical characterisation of a novel mutation in POLG associated with Alpers syndrome

André Schaller1*, Dagmar Hahn2, Christopher B Jackson1, Ilse Kern3, Christophe Chardot45, Dominique C Belli3, Sabina Gallati1 and Jean-Marc Nuoffer2

Author Affiliations

1 Division of Human Genetics, University Hospital Bern, Bern, Switzerland

2 Institute of Clinical Chemistry, University Hospital Bern, Bern, Switzerland

3 Department of Paediatrics, University of Geneva Children's Hospital, Geneva, Switzerland

4 Paediatric Surgery Unit, University of Geneva Children's Hospital, Geneva, Switzerland

5 Paediatric Surgery Unit, Hôpital Necker-Enfants malades, Paris, France

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BMC Neurology 2011, 11:4  doi:10.1186/1471-2377-11-4

Published: 14 January 2011

Additional files

Additional file 1:

Primer sequences for PCR amplification of POLG exons

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