About: Fatal mitochondrial myopathy with cytochrome-c-oxidase deficiency and subunit-restricted reduction of enzyme protein in two siblings: an autopsy-immunocytochemical study

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About: Fatal mitochondrial myopathy with cytochrome-c-oxidase deficiency and subunit-restricted reduction of enzyme protein in two siblings: an autopsy-immunocytochemical study Goto Sponge NotDistinct Permalink

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scientific article published on 01 July 1989

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в липні 1989 (uk) article scientifique publié en 1989 (fr) im Juli 1989 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xunetu de 1989 (ast) scientific article published on 01 July 1989 (en)
publication date	wds:Q69079080-C3880B3A-2E07-4687-8A8A-937D6C7D9EA2
publication date	1989-07-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q69079080-0F35A37C-1A6C-4BBA-BFD0-481292FF96CB wds:Q69079080-316BEBC9-1B3A-407A-818D-55D202AB5D07 wds:Q69079080-A386A5E8-7100-4280-B818-9E86C82C1694 wds:Q69079080-AFF124C6-C8C1-442B-81F4-ADEFC430FB89 wds:Q69079080-FB380AF0-111E-40CE-8C83-CE7E97EB7A58
author name string	B Kadenbach J Müller-Höcker D Pongratz G Hübner M Droste
rdfs:label	Fatal mitochondrial myopathy with cytochrome-c-oxidase deficiency and subunit-restricted reduction of enzyme protein in two siblings: an autopsy-immunocytochemical study (en) Fatal mitochondrial myopathy with cytochrome-c-oxidase deficiency and subunit-restricted reduction of enzyme protein in two siblings: an autopsy-immunocytochemical study (nl)
skos:prefLabel	Fatal mitochondrial myopathy with cytochrome-c-oxidase deficiency and subunit-restricted reduction of enzyme protein in two siblings: an autopsy-immunocytochemical study (en) Fatal mitochondrial myopathy with cytochrome-c-oxidase deficiency and subunit-restricted reduction of enzyme protein in two siblings: an autopsy-immunocytochemical study (nl)
name	Fatal mitochondrial myopathy with cytochrome-c-oxidase deficiency and subunit-restricted reduction of enzyme protein in two siblings: an autopsy-immunocytochemical study (en) Fatal mitochondrial myopathy with cytochrome-c-oxidase deficiency and subunit-restricted reduction of enzyme protein in two siblings: an autopsy-immunocytochemical study (nl)
title	wds:Q69079080-ABE2D04A-7383-47C7-B893-145BB00EAF01
title	Fatal mitochondrial myopathy with cytochrome-c-oxidase deficiency and subunit-restricted reduction of enzyme protein in two siblings: an autopsy-immunocytochemical study (en)
page(s)	wds:Q69079080-CE78126F-CCD6-41D8-90C4-DBCE2C38441F
page(s)	666-672
instance of	wds:Q69079080-D43E9636-E8C0-4C76-829E-4695541963B4
instance of	scholarly article
main subject	wds:Q69079080-1E8CA328-B9E1-4EB6-9C5F-853D55F57482 wds:Q69079080-D68DFB01-1FB1-45EA-B628-92FBF6F8A028
main subject	autopsy mitochondrial myopathy
PubMed ID	wds:Q69079080-08310EE4-6791-4EED-8EC7-5CFF594B0129
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/2472348
PubMed ID	2472348
published in	wds:Q69079080-0CD997B2-9C2F-46BA-8E4D-BB84806E6CFD
published in	Human Pathology
issue	wds:Q69079080-20389539-6958-4BBE-8AD4-E311DAE21323
volume	wds:Q69079080-16F9AF58-D402-46CA-BFED-C2728BCBE7C6
issue	7
volume	20
DOI	wds:Q69079080-40B93733-FD18-4FC8-9C00-25E23EAAF66E
DOI	http://dx.doi.org/10.1016/0046-8177(89)90154-8
DOI	10.1016/0046-8177(89)90154-8
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q69079080
is cites work of	Different in situ hybridization patterns of mitochondrial DNA in cytochrome c oxidase-deficient extraocular muscle fibres in the elderly Immunohistochemical analysis of muscle cytochrome c oxidase deficiency in children Mutations of mitochondrial DNA and human death Mitochondrial DNA depletion and fatal infantile hepatic failure due to mutations in the mitochondrial polymerase γ (POLG) gene: a combined morphological/enzyme histochemical and immunocytochemical/biochemical and molecular genetic study Defects of the respiratory chain in oxyphil and chief cells of the normal parathyroid and in hyperfunction Impaired Muscle Mitochondrial Biogenesis and Myogenesis in Spinal Muscular Atrophy. Mitochondrial quality control mechanisms as molecular targets in cardiac ageing Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies Clinical and molecular heterogeneity of cytochrome c oxidase deficiency in the newborn
is cites work of	wds:Q30447289-DDC21380-8FFC-482E-9AB7-37B89F6EEF4D wds:Q90452942-606037DB-31CA-4F3D-AD2F-01D5BC14FD86 wds:Q72071043-32016E53-06E3-4F9D-BE96-2C5593E30EB1 wds:Q71150649-50C1ECB7-DCC5-44FD-A0A1-12C4E628CF96 wds:Q72207091-8BD06C61-C409-4ECE-BA3E-8847413C41D2 wds:Q37094802-D32EF4C9-3433-4C3F-8BE9-E4AF3F23C360 wds:Q71523670-A1418608-86C2-49B5-AB5A-CC487DB7379D wds:Q68470001-977E0D0F-DA57-470E-83D4-BB8480B2547B wds:Q68262851-845CDCEE-1E30-46D9-9532-B4375B583511

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