MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder
about
Non-electron transfer chain mitochondrial defects differently regulate HIF-1α degradation and transcription.Lipoic acid metabolism and mitochondrial redox regulation.Genetic modifications of Mecr reveal a role for mitochondrial 2-enoyl-CoA/ACP reductase in placental development in mice.Detection of Selection Signatures in Chinese Landrace and Yorkshire Pigs Based on Genotyping-by-Sequencing Data.Protein moonlighting elucidates the essential human pathway catalyzing lipoic acid assembly on its cognate enzymes
P2860
MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder
description
2016 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2016
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im Dezember 2016 veröffentlichter wissenschaftlicher Artikel
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scientific journal article
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wetenschappelijk artikel (gepubliceerd op 2016/12/01)
@nl
наукова стаття, опублікована в грудні 2016
@uk
مقالة علمية (نشرت في ديسمبر 2016)
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name
MECR Mutations Cause Childhood ...... Fatty Acid Synthesis Disorder
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MECR Mutations Cause Childhood ...... Fatty Acid Synthesis Disorder
@en
type
label
MECR Mutations Cause Childhood ...... Fatty Acid Synthesis Disorder
@ast
MECR Mutations Cause Childhood ...... Fatty Acid Synthesis Disorder
@en
prefLabel
MECR Mutations Cause Childhood ...... Fatty Acid Synthesis Disorder
@ast
MECR Mutations Cause Childhood ...... Fatty Acid Synthesis Disorder
@en
P2093
P2860
P50
P921
P1476
MECR Mutations Cause Childhood ...... Fatty Acid Synthesis Disorder
@en
P2093
Alexander J. Kastaniotis
Allison Gregory
Alvit Veber
Andreea Nissenkorn
Annick Raas-Rothschild
Bruria Ben-Zeev
Caleb Rogers
Celeste Panteghini
Chen Hoffmann
Davide Tonduti
P2860
P304
P356
10.1016/J.AJHG.2016.09.021
P407
P577
2016-12-01T00:00:00Z