Corrigendum: Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations

Sara Brito¹, Kyle Thompson², Jaume Campistol³, Jaime Colomer⁴, Steven A Hardy², Langping He², Ana Fernández-Marmiesse⁵, Lourdes Palacios⁶, Cristina Jou⁷, Cecilia Jiménez-Mallebrera³, Judith Armstrong⁸, Raquel Montero⁹, Rafael Artuch⁹, Christin Tischner¹⁰, Tina Wenz¹¹, Robert McFarland², Robert W Taylor²

Affiliations

¹ Serviço de Pediatria, Centro Hospitalar de Leiria, Hospital de Santo André Leiria, Portugal ; Neuromuscular Unit, Neuropaediatrics Department, Hospital Sant Joan de Déu Barcelona, Spain.
² Wellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University Newcastle upon Tyne, UK.
³ Neuromuscular Unit, Neuropaediatrics Department, Hospital Sant Joan de Déu Barcelona, Spain ; Centro de Investigación Biomédica en Red de Enfermedades Raras, Instituto de Salud Carlos III Barcelona, Spain.
⁴ Neuromuscular Unit, Neuropaediatrics Department, Hospital Sant Joan de Déu Barcelona, Spain.
⁵ Diagnosis and Treatment Unit for Inborn Errors of Metabolism, Hospital Clínico Universitario de Santiago de Compostela La Coruña, Spain.
⁶ Progenika Biopharma a Grifols Company Derio, Spain.
⁷ Pathology Department, Hospital Sant Joan de Déu Esplugues Barcelona, Spain.
⁸ Centro de Investigación Biomédica en Red de Enfermedades Raras, Instituto de Salud Carlos III Barcelona, Spain ; Biochemical, Genetics and Rett Unit, Laboratory Department, Hospital Sant Joan de Déu Esplugues Barcelona, Spain.
⁹ Centro de Investigación Biomédica en Red de Enfermedades Raras, Instituto de Salud Carlos III Barcelona, Spain ; Biochemical Department, Hospital Sant Joan de Déu Esplugues Barcelona, Spain.
¹⁰ Cluster of Excellence, Cellular Stress Responses in Aging-Associated Diseases, Institute for Genetics, University of Cologne Cologne, Germany.
¹¹ Cluster of Excellence, Cellular Stress Responses in Aging-Associated Diseases, Institute for Genetics, University of Cologne Cologne, Germany ; German Network for Mitochondrial Disorders Munich, Germany.

PMID: 26284110
PMCID: PMC4516972
DOI: 10.3389/fgene.2015.00254

Published Erratum

Corrigendum: Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations

Sara Brito et al. Front Genet. 2015.

. 2015 Jul 28:6:254.

doi: 10.3389/fgene.2015.00254. eCollection 2015.

Authors

Affiliations

¹ Serviço de Pediatria, Centro Hospitalar de Leiria, Hospital de Santo André Leiria, Portugal ; Neuromuscular Unit, Neuropaediatrics Department, Hospital Sant Joan de Déu Barcelona, Spain.
² Wellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University Newcastle upon Tyne, UK.
³ Neuromuscular Unit, Neuropaediatrics Department, Hospital Sant Joan de Déu Barcelona, Spain ; Centro de Investigación Biomédica en Red de Enfermedades Raras, Instituto de Salud Carlos III Barcelona, Spain.
⁴ Neuromuscular Unit, Neuropaediatrics Department, Hospital Sant Joan de Déu Barcelona, Spain.
⁵ Diagnosis and Treatment Unit for Inborn Errors of Metabolism, Hospital Clínico Universitario de Santiago de Compostela La Coruña, Spain.
⁶ Progenika Biopharma a Grifols Company Derio, Spain.
⁷ Pathology Department, Hospital Sant Joan de Déu Esplugues Barcelona, Spain.
⁸ Centro de Investigación Biomédica en Red de Enfermedades Raras, Instituto de Salud Carlos III Barcelona, Spain ; Biochemical, Genetics and Rett Unit, Laboratory Department, Hospital Sant Joan de Déu Esplugues Barcelona, Spain.
⁹ Centro de Investigación Biomédica en Red de Enfermedades Raras, Instituto de Salud Carlos III Barcelona, Spain ; Biochemical Department, Hospital Sant Joan de Déu Esplugues Barcelona, Spain.
¹⁰ Cluster of Excellence, Cellular Stress Responses in Aging-Associated Diseases, Institute for Genetics, University of Cologne Cologne, Germany.
¹¹ Cluster of Excellence, Cellular Stress Responses in Aging-Associated Diseases, Institute for Genetics, University of Cologne Cologne, Germany ; German Network for Mitochondrial Disorders Munich, Germany.

PMID: 26284110
PMCID: PMC4516972
DOI: 10.3389/fgene.2015.00254

Abstract

[This corrects the article on p. 102 in vol. 6, PMID: 25852744.].

Keywords: GFM1; brain MRI; encephalopathy; mitochondrial disorders; mtEFG1.

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Erratum for

Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations.
Brito S, Thompson K, Campistol J, Colomer J, Hardy SA, He L, Fernández-Marmiesse A, Palacios L, Jou C, Jiménez-Mallebrera C, Armstrong J, Montero R, Artuch R, Tischner C, Wenz T, McFarland R, Taylor RW. Brito S, et al. Front Genet. 2015 Mar 23;6:102. doi: 10.3389/fgene.2015.00102. eCollection 2015. Front Genet. 2015. PMID: 25852744 Free PMC article.

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Corrigendum: Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations

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Corrigendum: Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations

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