Wikidata

(Q57970896)

English

NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe

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title
NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe (English)
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author
Bernard Sablonniere
object named as
Bernard Sablonniere
series ordinal
9
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Giovanni Stevanin
object named as
Giovanni Stevanin
series ordinal
12
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Alexandra Durr
series ordinal
3
object named as
Alexandra Durr
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Alexis Brice
series ordinal
11
object named as
Alexis Brice
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Christel Depienne
series ordinal
5
object named as
Christel Depienne
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Sylvie Forlani
series ordinal
6
object named as
Sylvie Forlani
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Stephan Klebe
series ordinal
1
object named as
Stephan Klebe
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Sandrine Poea-Guyon
series ordinal
7
object named as
Sandrine Poea-Guyon
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Tanya Stojkovic
series ordinal
4
object named as
Tanya Stojkovic
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Isabelle Vuillaume
series ordinal
8
object named as
Isabelle Vuillaume
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Arnaud Lacour
series ordinal
2
object named as
Arnaud Lacour
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Patrick Vermersch
series ordinal
10
object named as
Patrick Vermersch
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publication date
5 January 2007
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volume
8
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issue
2
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page(s)
155-157
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cites work

Identifiers

PubMed ID
17205300
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