A genetic mimic of cerebral palsy: Homozygous NFU1 mutation with marked intrafamilial phenotypic variation
- 1 November 2020
- journal article
- research article
- Published by Elsevier in Brain and Development
- Vol. 42 (10) , 756-761
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Understanding the Mechanism of [4Fe-4S] Cluster Assembly on Eukaryotic Mitochondrial and Cytosolic AconitaseInorganic Chemistry, 2019
- Understanding the molecular basis for multiple mitochondrial dysfunctions syndrome 1 (MMDS1): impact of a disease‐causing Gly189Arg substitution on NFU1The FEBS Journal, 2017
- Understanding the Molecular Basis of Multiple Mitochondrial Dysfunctions Syndrome 1 (MMDS1)—Impact of a Disease-Causing Gly208Cys Substitution on Structure and Activity of NFU1 in the Fe/S Cluster Biosynthetic PathwayJournal of Molecular Biology, 2017
- Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiencyFrontiers in Genetics, 2015
- New spastic paraplegia phenotype associated to mutation of NFU1Orphanet Journal of Rare Diseases, 2015
- Cavitating leukoencephalopathy with multiple mitochondrial dysfunction syndrome and NFU1 mutationsFrontiers in Genetics, 2014
- Leukoencephalopathy with cysts and hyperglycinemia may result from NFU1 deficiencyMitochondrion, 2014
- A Fatal Mitochondrial Disease Is Associated with Defective NFU1 Function in the Maturation of a Subset of Mitochondrial Fe-S ProteinsThe American Journal of Human Genetics, 2011
- Mutations in Iron-Sulfur Cluster Scaffold Genes NFU1 and BOLA3 Cause a Fatal Deficiency of Multiple Respiratory Chain and 2-Oxoacid Dehydrogenase EnzymesThe American Journal of Human Genetics, 2011
- A Novel Syndrome Affecting Multiple Mitochondrial Functions, Located by Microcell-Mediated Transfer to Chromosome 2p14-2p13The American Journal of Human Genetics, 2001