Reply: Infantile Leigh-like syndrome caused by SLC19A3 mutations is a treatable disease

Brain. 2014 Sep;137(Pt 9):e297. doi: 10.1093/brain/awu130. Epub 2014 May 30.

Authors

Marjo S van der Knaap¹, Sietske H Kevelam²

Affiliations

¹ 1 Department of Child Neurology and Neuroscience Campus Amsterdam, VU University Medical Centre, Amsterdam, The Netherlands2 Department of Functional Genomics, VU University, De Boelelaan 1085, 1081 HV Amsterdam, The Netherlands [email protected].
² 1 Department of Child Neurology and Neuroscience Campus Amsterdam, VU University Medical Centre, Amsterdam, The Netherlands.

PMID: 24878500
DOI: 10.1093/brain/awu130

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't
Comment

MeSH terms

Brain Chemistry / genetics*
Exome / genetics*
Female
Humans
Leigh Disease / genetics*
Leigh Disease / pathology*
Male
Membrane Transport Proteins / genetics*
Mutation / genetics*

Substances

Membrane Transport Proteins