Deficiency in SLC25A1, Encoding the Mitochondrial Citrate Carrier, Causes Combined D-2- and L-2-Hydroxyglutaric Aciduria-Reference-Cited by-同舟云学术

Deficiency in SLC25A1, Encoding the Mitochondrial Citrate Carrier, Causes Combined D-2- and L-2-Hydroxyglutaric Aciduria

Published:2013-04 Issue:4 Volume:92 Page:627-631
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Nota Benjamin,Struys Eduard A.,Pop Ana,Jansen Erwin E.,Fernandez Ojeda Matilde R.,Kanhai Warsha A.,Kranendijk Martijn,van Dooren Silvy J.M.,Bevova Marianna R.,Sistermans Erik A.,Nieuwint Aggie W.M.,Barth Magalie,Ben-Omran Tawfeg,Hoffmann Georg F.,de Lonlay Pascale,McDonald Marie T.,Meberg Alf,Muntau Ania C.,Nuoffer Jean-Marc,Parini Rossella,Read Marie-Hélène,Renneberg Axel,Santer René,Strahleck Thomas,van Schaftingen Emile,van der Knaap Marjo S.,Jakobs Cornelis,Salomons Gajja S.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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