Search filters

Authors whose works are in public domain in at least one jurisdiction

List of works by Agnès Delahodde

CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizures

scientific article

Contribution of ERMES subunits to mature peroxisome abundance

scientific article published on 25 March 2019

Mutations in human lipoyltransferase gene LIPT1 cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase

scientific article published on 17 December 2013

Mutations in the tricarboxylic acid cycle enzyme, aconitase 2, cause either isolated or syndromic optic neuropathy with encephalopathy and cerebellar atrophy

scientific article published on 28 October 2014

Paulina is supported by:

About Paulina

Help