Wikidata

(Q24563811)

English

Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60

scientific article

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Statements

instance of
scholarly article
0 references
case report
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title
Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60 (English)
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author name string
Jens Jacob Hansen
series ordinal
1
author given names
Jens Jacob
author last names
Hansen
1 reference
stated in
PubMed
PubMed ID
11898127
retrieved
18 November 2023
Costa Georgopoulos
series ordinal
4
author given names
Costa
author last names
Georgopoulos
1 reference
stated in
PubMed
PubMed ID
11898127
retrieved
18 November 2023
Debbie Ang
series ordinal
5
author given names
Debbie
author last names
Ang
1 reference
stated in
PubMed
PubMed ID
11898127
retrieved
18 November 2023
Marit Nyholm Nielsen
series ordinal
6
author given names
Marit Nyholm
author last names
Nielsen
1 reference
stated in
PubMed
PubMed ID
11898127
retrieved
18 November 2023
Niels Gregersen
series ordinal
10
author given names
Niels
author last names
Gregersen
1 reference
stated in
PubMed
PubMed ID
11898127
retrieved
18 November 2023
publication date
May 2002
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volume
70
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page(s)
1328-32
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issue
5
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cites work

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