About: Chronic progressive external ophthalmoplegia caused by an m.4267A

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About: Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNAIle Goto Sponge Distinct Permalink

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scientific article published on 02 November 2007

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в листопаді 2007 (uk) article scientifique publié en 2007 (fr) im November 2007 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en payares de 2007 (ast) scientific article published on 02 November 2007 (en)
publication date	wds:Q62671290-44039B1C-7EBD-47C3-BF66-3AADE7D6B50D
publication date	2007-11-02 00:00:00Z (xsd:dateTime)
exact match	wds:Q62671290-FDCF446F-DC4B-4840-B0BB-ABBCA5244587
exact match	https://scigraph.springernature.com/pub.10.1007/s00415-007-0608-6
cites work	wds:Q62671290-895779A9-B707-4B72-93A3-DB0BB129F144 wds:Q62671290-B3E7C4A0-2B02-42FA-A805-A33D67645B37 wds:Q62671290-B55F5902-17AE-480B-9264-32481FA08E05 wds:Q62671290-B8783252-FDA1-4D6D-95F7-072EE153528C
cites work	MITOMAP: a human mitochondrial genome database--2004 update Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome. Measurement of the Energy-Generating Capacity of Human Muscle Mitochondria: Diagnostic Procedure and Application to Human Pathology A novel mitochondrial DNA tRNA(Ile) (A4267G) mutation in a sporadic patient with mitochondrial myopathy.
author name string	wds:Q62671290-DC5D37DD-F365-48F0-A1AF-26D83984EE82 wds:Q62671290-DE907EE1-7D92-4C19-80B3-51E206A86B5D
author name string	Gea Drost Frans A Hol
rdfs:label	Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNAIle (en) Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNAIle (nl)
skos:prefLabel	Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNAIle (en) Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNAIle (nl)
name	Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNAIle (en) Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNAIle (nl)
author	wds:Q62671290-0D2915E3-C906-4EE1-A119-7E2659993114 wds:Q62671290-0F938C50-7DF5-4A0C-B4CF-D770C3B43378 wds:Q62671290-2B890BFD-EDC7-459A-A9FB-4678118FABA7 wds:Q62671290-63C57B8C-DD01-4538-8A58-E93D280A65C4 wds:Q62671290-8A79E00D-FB5B-4589-A1EA-44AA70ADE583
author	Lambert P van den Heuvel Baziel van Engelen Richard J Rodenburg Bart M G Smits Henk J Ter Laak
title	wds:Q62671290-EF8A66B1-F3EB-4CD1-8BE4-CC03B10B94D5
title	Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNAIle (en)
page(s)	wds:Q62671290-D57FED3D-3A92-4330-869E-DC0E3936B39B
page(s)	1614-1615
instance of	wds:Q62671290-212960DF-20CB-4AB3-AE92-21D11F2AE16B
instance of	scholarly article
main subject	wds:Q62671290-0B80EF1A-D8EC-4D4D-8D0A-46B46441D3BC wds:Q62671290-33B5B0D8-0CFB-469E-9ACF-FF23E8342C04
main subject	mitochondrion chronic progressive external ophthalmoplegia
PubMed ID	wds:Q62671290-984C66BC-3F03-4D52-B01A-83567214C6EC
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17965958
PubMed ID	17965958
published in	wds:Q62671290-B495C78E-F7EC-486D-92D2-AC9CE18EC04A
published in	Journal of Neurology
issue	wds:Q62671290-D2A9B4AC-8630-4098-BE54-62D883431233
volume	wds:Q62671290-B4E65A7B-A324-4E69-808B-D1B07E6F3823
issue	11
volume	254
DOI	wds:Q62671290-ACD17758-FD2F-407A-B0EA-F497D3D1DC7E
DOI	http://dx.doi.org/10.1007/S00415-007-0608-6
DOI	10.1007/S00415-007-0608-6
Dimensions Publication ID	wds:Q62671290-B1EB8929-2AEC-48B4-8EC5-D3B363255746
Dimensions Publication ID	1045190799
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q62671290
is cites work of	Recurrent myoglobinuria in a sporadic patient with a novel mitochondrial DNA tRNA(Ile) mutation Peripheral neuropathy predicts nuclear gene defect in patients with mitochondrial ophthalmoplegia A novel mutation in the tRNAIle gene (MTTI) affecting the variable loop in a patient with chronic progressive external ophthalmoplegia (CPEO).
is cites work of	wds:Q37533307-CC4351AE-5669-430D-94D7-59A470386643 wds:Q33737397-1A2D6F56-8A1A-43C0-A73D-C13945567D58 wds:Q34555959-6012BB20-1FEC-4116-897D-4A8651374D86

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