Correspondence to: “Heterozygous mutation in the X chromosomal NDUFA1 gene in a girl with complex I deficiency” and “A novel NDUFA1 mutation leads to progressive mitochondrial complex I- specific neurodegenerative disease”

Detalles Bibliográficos
Autores principales: Xu, Jack Junchi, Østergaard, Elsebet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537428/
https://www.ncbi.nlm.nih.gov/pubmed/28794991
http://dx.doi.org/10.1016/j.ymgmr.2017.07.008
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author Xu, Jack Junchi
Østergaard, Elsebet
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Østergaard, Elsebet
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spelling pubmed-55374282017-08-09 Correspondence to: “Heterozygous mutation in the X chromosomal NDUFA1 gene in a girl with complex I deficiency” and “A novel NDUFA1 mutation leads to progressive mitochondrial complex I- specific neurodegenerative disease” Xu, Jack Junchi Østergaard, Elsebet Mol Genet Metab Rep Letter to the Editor Elsevier 2017-07-26 /pmc/articles/PMC5537428/ /pubmed/28794991 http://dx.doi.org/10.1016/j.ymgmr.2017.07.008 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Letter to the Editor
Xu, Jack Junchi
Østergaard, Elsebet
Correspondence to: “Heterozygous mutation in the X chromosomal NDUFA1 gene in a girl with complex I deficiency” and “A novel NDUFA1 mutation leads to progressive mitochondrial complex I- specific neurodegenerative disease”
title Correspondence to: “Heterozygous mutation in the X chromosomal NDUFA1 gene in a girl with complex I deficiency” and “A novel NDUFA1 mutation leads to progressive mitochondrial complex I- specific neurodegenerative disease”
title_full Correspondence to: “Heterozygous mutation in the X chromosomal NDUFA1 gene in a girl with complex I deficiency” and “A novel NDUFA1 mutation leads to progressive mitochondrial complex I- specific neurodegenerative disease”
title_fullStr Correspondence to: “Heterozygous mutation in the X chromosomal NDUFA1 gene in a girl with complex I deficiency” and “A novel NDUFA1 mutation leads to progressive mitochondrial complex I- specific neurodegenerative disease”
title_full_unstemmed Correspondence to: “Heterozygous mutation in the X chromosomal NDUFA1 gene in a girl with complex I deficiency” and “A novel NDUFA1 mutation leads to progressive mitochondrial complex I- specific neurodegenerative disease”
title_short Correspondence to: “Heterozygous mutation in the X chromosomal NDUFA1 gene in a girl with complex I deficiency” and “A novel NDUFA1 mutation leads to progressive mitochondrial complex I- specific neurodegenerative disease”
title_sort correspondence to: “heterozygous mutation in the x chromosomal ndufa1 gene in a girl with complex i deficiency” and “a novel ndufa1 mutation leads to progressive mitochondrial complex i- specific neurodegenerative disease”
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537428/
https://www.ncbi.nlm.nih.gov/pubmed/28794991
http://dx.doi.org/10.1016/j.ymgmr.2017.07.008
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AT østergaardelsebet correspondencetoheterozygousmutationinthexchromosomalndufa1geneinagirlwithcomplexideficiencyandanovelndufa1mutationleadstoprogressivemitochondrialcomplexispecificneurodegenerativedisease

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