ETFDH (English Wikipedia)
Analysis of information sources in references of the Wikipedia article "ETFDH" in English language version.
refsWebsite
Global rank
English rank
1,626th place
1,007th place
11th place
8th place
5,673rd place
6,418th place
1,010th place
612th place
creativecommons.org (Global: 1,010th place; English: 612th place)
- "ETFDH - Electron transfer flavoprotein-ubiquinone oxidoreductase, mitochondrial precursor - Homo sapiens (Human) - STXBP1 gene & protein". www.uniprot.org. Retrieved 2018-08-29.
This article incorporates text available under the CC BY 4.0 license.
doi.org (Global: 2nd place; English: 2nd place)
- Olsen RK, Andresen BS, Christensen E, Bross P, Skovby F, Gregersen N (July 2003). "Clear relationship between ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency". Human Mutation. 22 (1): 12–23. doi:10.1002/humu.10226. PMID 12815589. S2CID 24730356.
- "UniProt: the universal protein knowledgebase". Nucleic Acids Research. 45 (D1): D158–D169. January 2017. doi:10.1093/nar/gkw1099. PMC 5210571. PMID 27899622.
- Liang WC, Lin YF, Liu TY, Chang SC, Chen BH, Nishino I, Jong YJ (September 2017). "Neurite growth could be impaired by ETFDH mutation but restored by mitochondrial cofactors". Muscle & Nerve. 56 (3): 479–485. doi:10.1002/mus.25501. PMID 27935074. S2CID 38848222.
ebi.ac.uk (Global: 5,849th place; English: 7,886th place)
- IntAct. "ETFDH interactions". www.ebi.ac.uk. Retrieved 2018-09-05.
ensembl.org (Global: 1,626th place; English: 1,007th place)
May2017.archive.ensembl.org
- GRCh38: Ensembl release 89: ENSG00000171503 – Ensembl, May 2017
- GRCm38: Ensembl release 89: ENSMUSG00000027809 – Ensembl, May 2017
nih.gov (Global: 4th place; English: 4th place)
ncbi.nlm.nih.gov
- "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "Entrez Gene: ETFDH electron-transferring-flavoprotein dehydrogenase".
- "UniProt: the universal protein knowledgebase". Nucleic Acids Research. 45 (D1): D158–D169. January 2017. doi:10.1093/nar/gkw1099. PMC 5210571. PMID 27899622.
pubmed.ncbi.nlm.nih.gov
- Olsen RK, Andresen BS, Christensen E, Bross P, Skovby F, Gregersen N (July 2003). "Clear relationship between ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency". Human Mutation. 22 (1): 12–23. doi:10.1002/humu.10226. PMID 12815589. S2CID 24730356.
- "UniProt: the universal protein knowledgebase". Nucleic Acids Research. 45 (D1): D158–D169. January 2017. doi:10.1093/nar/gkw1099. PMC 5210571. PMID 27899622.
- Liang WC, Lin YF, Liu TY, Chang SC, Chen BH, Nishino I, Jong YJ (September 2017). "Neurite growth could be impaired by ETFDH mutation but restored by mitochondrial cofactors". Muscle & Nerve. 56 (3): 479–485. doi:10.1002/mus.25501. PMID 27935074. S2CID 38848222.
omim.org (Global: 4,380th place; English: 4,305th place)
semanticscholar.org (Global: 11th place; English: 8th place)
api.semanticscholar.org
- Olsen RK, Andresen BS, Christensen E, Bross P, Skovby F, Gregersen N (July 2003). "Clear relationship between ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency". Human Mutation. 22 (1): 12–23. doi:10.1002/humu.10226. PMID 12815589. S2CID 24730356.
- Liang WC, Lin YF, Liu TY, Chang SC, Chen BH, Nishino I, Jong YJ (September 2017). "Neurite growth could be impaired by ETFDH mutation but restored by mitochondrial cofactors". Muscle & Nerve. 56 (3): 479–485. doi:10.1002/mus.25501. PMID 27935074. S2CID 38848222.
uniprot.org (Global: 5,673rd place; English: 6,418th place)
- "ETFDH - Electron transfer flavoprotein-ubiquinone oxidoreductase, mitochondrial precursor - Homo sapiens (Human) - STXBP1 gene & protein". www.uniprot.org. Retrieved 2018-08-29. This article incorporates text available under the CC BY 4.0 license.