Mutations inSDHDlead to autosomal recessive encephalomyopathy and isolated mitochondrial complex II deficiency

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Title:: Mutations inSDHDlead to autosomal recessive encephalomyopathy and isolated mitochondrial complex II deficiency
Document type:: Zeitschriftenaufsatz
Author(s):: Jackson, Christopher Benjamin; Nuoffer, Jean-Marc; Hahn, Dagmar; Prokisch, Holger; Haberberger, Birgit; Gautschi, Matthias; Häberli, Annemarie; Gallati, Sabina; Schaller, André
Journal title:: Journal of Medical Genetics
Year:: 2013
Journal volume:: 51
Journal issue:: 3
Pages contribution:: 170-175
Fulltext / DOI:: doi:10.1136/jmedgenet-2013-101932
Publisher:: BMJ
E-ISSN:: 0022-25931468-6244
Notes:: Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich. This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively.
Date of publication:: 23.12.2013
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