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Results of search for 'au:"Rantamäki, M"'
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Authors
Al Memar, A
Cormand, B
De Jonghe, P
Hackman, P
Hakamies, L
Hietala, M
Juvonen, V
Kaakkola, S
Krahe, R
Luoma, P
Löfgren, A
Martin, J J
Mononen, I
Paetau, A
Penttinen, M
Päivärinta, M
Rantamäki, M
Rinne, J O
Suomalainen, A
Udd, B
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Adolescent
Adult
Aged
Aged, 80 and over
Amino Acid Substitution
Ataxia
Blotting, Southern
DNA Polymerase gamma
DNA-Directed DNA Polymerase
Female
Finland
Genes, Recessive
Humans
Magnetic Resonance Imaging
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Middle Aged
Pedigree
diagnosis
genetics
pathology
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English
Your search returned 4 results.
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1.
Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish family.
[electronic resource]
by
Rantamäki, M
Krahe, R
Paetau, A
Cormand, B
Mononen, I
Udd, B
Producer:
20011018
In:
Neurology
vol. 57
Online resources:
Available from publisher's website
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No items available.
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2.
Do carriers of POLG mutation W748S have disease manifestations?
[electronic resource]
by
Rantamäki, M
Luoma, P
Virta, J J
Rinne, J O
Paetau, A
Suomalainen, A
Udd, B
Producer:
20080122
In:
Clinical genetics
vol. 72
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3.
Clinical and genetic findings in Finnish ataxia patients with the spinocerebellar ataxia 8 repeat expansion.
[electronic resource]
by
Juvonen, V
Hietala, M
Päivärinta, M
Rantamäki, M
Hakamies, L
Kaakkola, S
Vierimaa, O
Penttinen, M
Savontaus, M L
Producer:
20001016
In:
Annals of neurology
vol. 48
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No items available.
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4.
POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement.
[electronic resource]
by
Van Goethem, G
Luoma, P
Rantamäki, M
Al Memar, A
Kaakkola, S
Hackman, P
Krahe, R
Löfgren, A
Martin, J J
De Jonghe, P
Suomalainen, A
Udd, B
Van Broeckhoven, C
Producer:
20050608
In:
Neurology
vol. 63
Online resources:
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