Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease (Q24309083)

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12 November 2019

title

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease (English)

1 reference

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SPG7 matrix AAA peptidase subunit, paraplegin

12 November 2019

main subject

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GOA release 2020-03-11

unfolded protein binding

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GOA release 2020-03-11

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12 November 2019

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12 November 2019

M De Fusco

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12 November 2019

S Ciarmatori

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M Zeviani

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12 November 2019

G De Michele

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A Filla

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12 November 2019

S Cocozza

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12 November 2019

R Marconi

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12 November 2019

A Dürr

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12 November 2019

B Fontaine

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12 November 2019

P Fernandez

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12 November 2019

language of work or name

English

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publication date

1 June 1998

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volume

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issue

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page(s)

973-983

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Basic local alignment search tool

12 November 2019

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Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p

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Consolidated OpenCitations Corpus – April 2017

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12 November 2019

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Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json