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Siri L. Rydning
Siri L. Rydning
University of Oslo
Ataxia
Spastic
Genetics
Medicine
KIF1A
2
Papers
53
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Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia.
2017
PLOS ONE
Zafar Iqbal
Siri L. Rydning
Iselin Marie Wedding
Jeanette Koht
Lasse Pihlstrøm
Aina Rengmark
Sandra Pilar Henriksen
Chantal M. E. Tallaksen
Mathias Toft
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Citations (43)
A founder mutation p.H701P identified as a major cause of SPG7 in Norway
2016
European Journal of Neurology
Siri L. Rydning
Iselin Marie Wedding
Jeanette Koht
Maninder Singh Chawla
Ane-Marte Øye
Ying Sheng
Magnus Dehli Vigeland
Kaja Kristine Selmer
Chantal M. E. Tallaksen
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Citations (10)
1